Used Sterilization for sale (196)

Year of construction: 2014, condition: good (used), Mechatronics RPU-2100R Reagent Production Unit The Mechatronics RPU-2100R is a reagent production unit used in hematology to optimize reagent logistics in laboratories. The unit is manufactured by RR Mechatronics and is often used in combination with hematology analyzers from Sysmex. Purpose and Function The RPU-2100R (Reagent Production Unit) is used to automatically dilute concentrated reagents (such as Cellpack S Conc.) and produce large quantities of ready-to-use reagent on-site in the laboratory. The RPU-2100R is a standalone unit with all components housed in a single, enclosed enclosure. The enclosure features removable, epoxy-coated metal covers. All external connections and the ON/OFF switch are located on the rear of the unit. All user-serviceable and replaceable components are accessible via the front door. The cart for the Cellpack concentrate (e.g., Cellpack®-S Conc.) can be attached to any three sides of the unit. Features and Capacities The RPU-2100R focuses on optimizing reagent management for high-throughput laboratories: Reagent Concentrates: Uses Cellpack S Conc. in 10L and 20L containers. Throughput per Concentrate: Up to 8,250 complete blood counts per month can be performed with a 10L container without reagent changes. Up to 16,500 complete blood counts per month are possible with a 20L container. Shelf Life: Once opened, the reconstituted reagent has a shelf life of 30 days. Manufacturer: RR Mechatronics Model: RPU-2100R Catalog Number: NARP109010 External Connections Power Supply, Euro Plug Ethernet/USB (NARP109010 only) RJ45/USB-B RS-232 (NARP109000 only) 9-Pin SUB D Connector External Connections (Liquids) Water Connection: G ¾" Thread Reagent Dispensing Connections (4x) Push-in Hose Connection, 6 mm Outer Diameter Waste Connection (1x) Hose Barb, 12 mm Inner Diameter Reagent Concentrate Maximum Dimensions: 390 x 260 x 300 mm (W x D x H) Reagent: SYSMEX Cellpack Concentrate Peak Reagent Dispensing Rate: 0.5 Liters/Minute for 6 Minutes max. (at (with full reservoir and overflow tank and new pre-filter) 1 liter/minute, 2 minutes max. Filtration: Air filter, bacteria filter, pore size 0.2 µm Liquid pre-filter: Particle filter (sterilized), pore size 0.8+0.45 µm, self-venting Liquid final filter: Bacteria filter (sterilized), pore size 0.2 µm, self-venting System dimensions: Width: 500 mm Height: 700 mm Depth: 430 mm Weight: approx. 50 kg Water tank volume: 2.5 liters Reservoir: 2.5 liters Mixing tank: 0.6 liters Overflow tank: 0.6 liters Language selection available: German, English, Spanish, French, Hungarian, Italian, Dutch, Swedish Swedish (spreadable) Rcsdpfxjyk U Dwe Ahcef Voltage: 230 VAC (+/- 10%) Frequency: 50-60 Hz Year of manufacture: 2014 Find more items – new and used – in our shop! International shipping costs available upon request!

Condition: used, This listing is for the Bioquell Microflow Advanced Bio Safety Cabinet Class 2 The unit is in full working condition and is ready for immediate use The Bioquell Microflow Advanced is a high-performance Class II Biological Safety Cabinet (BSC) engineered to provide the highest level of protection for the operator, the environment, and your sensitive samples. It is the gold standard for labs handling moderate-to-high risk biological agents. Key Features & Benefits: Dual Protection: Utilizes advanced laminar airflow and HEPA filtration to create a sterile work zone while protecting the user from hazardous aerosols. Intuitive Control System: Features a clear digital display and easy-to-use interface for monitoring airflow velocities and filter status in real-time. Rcedpfx Ahoyu Trnjcsf Ergonomic Design: The angled front sash and bright internal lighting reduce glare and physical strain during long sessions of microscopy or pipetting. Safe Change Technology: Designed for easy and safe filter replacements, minimizing downtime and maintenance risks. Versatile Lab Utility: Ideal for microbiology, cell culture, and pharmaceutical research where contamination control is non-negotiable.

Condition: used, This listing is for the Palltronic Flowstar IV The unit is in full working condition and is ready for immediate use Palltronic Flowstar IV Filter Integrity Testing Instrument (and variants like Pall FFS04 S Palltronic Flowstar IV Filter Integrity Test Instrument / Pall Flowstar IV FFS04 Filter Integrity Tester) are precision filter integrity test instruments designed to check whether sterilising-grade membrane filters and associated assemblies have defects (like leaks or incomplete retention) before they are used in critical processes — particularly in pharmaceutical manufacturing and biotech Typical Uses Rodeyfhdmepfx Ahcocf These instruments are most commonly used in environments where sterility is critical: Final filtration before sterile drug product filling. Leak testing of single-use assemblies and filter housings. Quality control in vaccine production, biologics manufacturing, and related biotech workflows.

Condition: new, Year of construction: 2020, functionality: fully functional, machine/vehicle number: BH6723-BH1001, tank capacity: 1,000 l, Equipment: documentation/manual, BRINOX 1,000 L Pre-Fill Tank – 1.4435 – Double Jacket – PED Cat. IV Module G – TÜV – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMMBI-1000 Tag No.: BH6723-BH1001 Serial No.: 1003454 Year of Manufacture: 2020 CE Marking: CE 0036 Condition: As new / unused TECHNICAL DATA Product type: Pre-fill / process vessel Nominal volume: 1,000 L Total volume: 1,400 L Net weight: approx. 610–762 kg Product contact material: 1.4435 (AISI 316L) Permissible pressure PS: -1 / +3 bar Test pressure PT: 5.4 bar Permissible temperature TS: -10 / +150 °C Fluid group: 1 Design according to AD 2000 Pressure vessel in accordance with PED 2014/68/EU Category IV Module G – Individual inspection Notified body: TÜV SÜD Identification number: 0036 TÜV CERTIFICATION EU Declaration of Conformity (Module G) Certificate no.: Z-EU-SI-LJU-20-05-2702107-19125214 Inspection report no.: P-EU-SI-LJU-20-05-2702107-19125214 Final inspection in accordance with PED Annex I No. 3.2 carried out Pressure test in accordance with Annex I No. 3.2.2 carried out Acceptance without deviations Permissible load cycle count: 10,000 cycles (1.3 bar) Acceptance date: 20.05.2020 FAT – Factory Acceptance Test Complete works FAT carried out: • Pressure test • Visual inspection of weld seams • NDT testing (RT/PT) • Dimensional inspection • Surface roughness measurement (≤ 0.8 µm) • Calibration test • Documentation review FAT fully documented. DESIGN • Cylindrical, horizontal pressure vessel • Double jacket for heating/cooling • Internally electropolished • Pharmaceutical-grade weld finish • Manhole DN 500 • CIP connection • Safety valve • Pressure gauge • Multiple process and measuring nozzles • For pressurised and vacuum operation CONDITION • Never used in production • Factory tested • TÜV Module G certified • As-new industrial condition • No signs of use • Immediately available DOCUMENTATION Complete structured documentation available, including: • EU Declaration of Conformity • TÜV certificate with inspection report • TÜV design assessment • FAT protocols • Material certificates EN 10204 3.1 • WPS/WPQR and welders’ lists • NDT reports • Surface roughness protocols Rodpfxeykqmzo Ahcocf • Internal pressure test • Measurement reports • Calibration certificates • Parts list and drawings • Operating and maintenance manuals Digital documentation folder available. • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP installations • Biotechnology High-quality BRINOX pharmaceutical specification with PED Cat. IV Module G individual inspection by TÜV SÜD (CE 0036) and complete FAT documentation. Not a standard tank – tested project quality. Immediately available.

Condition: new, Miltenyi Biotec Sterile Filter Adapter 170-076-610 exp. 2026.02.24 - 50 boxes Rcjdpfxsvv Nqfe Ahcjf 5 pcs per box, price is for one box only.

Condition: used, Year of construction: 1999, Overview  The Sensometic vacuum filler was built by Krones in 1999. The offer also includes rinser, Alcoa cappers and a blocked labeler. The machines can be inspected at any time.   Technical details  Output  12,000 bottles/h with 0.7l glass bottle  10,000 bottles/h with 1.0l glass bottle  6,000 bottles/h with 1.5l PET bottle  Formats  0.7l glass bottle  1.0l glass bottle  1.5l PET bottle  Plastic closure  Screw cap 28 mm  Push-on cap  Label  Body, back, neck loop, neck ring  Bottling product  Raspberry and various fruit syrups   Special hesperide vinegar   Filling temperature: 25°C   Running direction: L-R   Siemens S5   Scope of delivery  Rinser | Krones | Variojet | 3-channel rinser; steam, sterile water, air  Vacuum filler | Krones | Sensometic |   Capper | Alcoa | PP 10 / 360   Capper | Alcoa | K 10 / 360  Cold glue labeler | Krones | Prontomatic   Redjukkvnepfx Ahcecf

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 1,000 l, Equipment: documentation/manual, BRINOX 1,000 L Pre-Fill Vessel – 1.4435 – Double Jacket – PED Cat. IV Module G – TÜV – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMMBI-1000 Tag No.: BH6725-BH1001 Serial No.: 1003455 Year of manufacture: 2020 CE Marking: CE 0036 Condition: As new / unused TECHNICAL SPECIFICATIONS Product type: Pre-fill / process vessel Nominal volume: 1,000 L Total volume: 1,400 L Rodoykt T Rjpfx Ahcecf Empty weight: 762 kg Product contact material: 1.4435 Permissible pressure (PS): -1 / +3 bar Test pressure (PT): 5.4 bar Permissible temperature (TS): -10 / +150 °C Fluid group: 1 Design according to AD 2000 Pressure vessel compliant with PED 2014/68/EU Category IV Module G – Single Unit Inspection Notified body: TÜV SÜD Notification number: 0036 FAT – Factory Acceptance Test Full factory FAT conducted and documented. Testing includes pressure test, NDT (non-destructive testing), dimensional inspection, surface roughness inspection, and documentation release. FEATURES • Cylindrical horizontal pressure vessel • Double jacket for heating/cooling • Interior electropolished • Pharmaceutical-grade welding • Manway DN500 • Multiple process and instrument connections • Safety valve • CIP connections • Suitable for pressure and vacuum operation CONDITION • Never used in production • TÜV Module G certified • As-new industrial condition • Immediately available DOCUMENTATION – complete and available Comprehensive structured documentation including: • EU Declaration of Conformity • TÜV certificate with inspection report • TÜV design assessment • FAT documentation • Material certificates • Welding lists and WPS/WPQR • NDT reports • Surface roughness protocol • Surface treatment report • Internal pressure test • Dimensional protocol • Calibration certificate (pressure gauge) • Component drawings • Assembly parts list • Operation and maintenance manuals (equipment & components) • Qualification certificates • Analysis certificates for welding consumables and shielding gases Complete digital documentation file available. APPLICATIONS • Pharmaceutical industry • WFI / PW • GMP-compliant plants • Sterile liquid processes • Biotechnology High-quality BRINOX pharmaceutical version with PED Cat. IV Module G single unit inspection by TÜV SÜD, complete FAT, and full technical documentation. Immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 3,500 l, Equipment: documentation/manual, BRINOX 3,500 L Storage Tank – 1.4404 – PED Module G – TÜV – FAT – 2020 – As New Rjdpfoylnppox Ahcscf Manufacturer: BRINOX d.o.o., Slovenia Type: SVBBH-3500 Tag no.: Serial number: 1003461 Year of manufacture: 2020 Condition: As new / unused BH6771-BH1001 Package 29 TECHNICAL DATA Product type: Storage tank / process vessel Nominal capacity: 3,500 liters Total volume: approx. 4,082 liters Empty weight: approx. 1,750 kg Material in contact with product: 1.4404 (AISI 316L) Internal surface: electropolished Surface roughness: tested according to roughness protocol (Ra ≤ 0.8 µm) Permissible pressure PS, vessel: -1 / +3 bar Test pressure PT, vessel: 5.6 bar Permissible pressure PS, jacket: -1 / +6 bar Test pressure PT, jacket: 10.8 bar Permissible temperature TS: -10 °C to +150 °C Fluid group: 2 Design according to AD 2000 Pressure vessel according to PED 2014/68/EU Category III Module G – single item inspection CE marking FAT – Factory Acceptance Test Full FAT inspection carried out on 26.08.2020. Documentation check: complete and released Welding documentation inspected and compliant Delta ferrite inspection conducted, no deviations Surface roughness checked and compliant All inspections rated “OK”. EXECUTION • Horizontal cylindrical pressure vessel • Dished heads • Multiple CIP connections on end face • CIP spray ball system • Manhole with round pressure cover • Pressure and temperature connections • Bottom discharge outlet • Stainless steel support legs • Pharmaceutical-grade weld seams DOCUMENTATION – fully available • EU Declaration of Conformity • TÜV certificate • Module G individual inspection • FAT protocols • Welding documentation • WPQR / WPS • 3.1 Material certificates • Non-destructive test reports • Delta ferrite test report • Roughness protocol • Dimensional accuracy report • Calibration certificates • Technical drawings • Parts list • Operating and maintenance manual Complete digital documentation folder available. CONDITION • Never in productive use • Stored item • Interior surface in absolutely as-new condition • No corrosion • No signs of use • As-new industrial condition • Immediately available SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP production facilities • Biotechnological applications SPECIAL FEATURE Custom-manufactured BRINOX pharmaceutical tank with full FAT acceptance, verified welding documentation, delta ferrite certification, documented surface roughness, and comprehensive PED Module G single-inspection. Not a standard tank – but pharmaceutical grade suitable for validation, with complete technical documentation throughout.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 9,000 l, Equipment: documentation/manual, BRINOX 9,000 L Wash Solution Tank – 316L – Jacketed – TÜV / PED – As New Manufacturer: BRINOX d.o.o. Tag No.: BH6751-BH1001 Package 31 Year: 2020 Condition: As new / unused Technical Data Product type: Wash solution tank Nominal volume: approx. 9,000 litres Wetted material: 1.4404 (AISI 316L) Design: Horizontal layout CE marking: available Pressure vessel in accordance with PED 2014/68/EU TÜV-inspected with acceptance report Jacket for heating/cooling available Designed for pharmaceutical applications Internal surface: • High-gloss polish • Pharmaceutical-grade weld seams • Documented surface quality Design / Equipment • Custom-built in 316L stainless steel • Large manway with pressure closure • Integrated CIP spray nozzles / cleaning pipes • Multiple clamp and flange connections • Instrument ports (pressure, temperature, sensors) • Robust lifting and carrying lugs • Heavy-duty industrial design • Pre-installed external piping and process connections • Excellent accessibility for maintenance and inspection The images clearly show the high-quality workmanship, the clean welding, and the mirror-polished product-contact internal surface. Condition • Never used in production • Inventory stock from project surplus • Absolutely clean interior • No corrosion • No signs of use • As-new industrial condition • Immediately available Suitable for • Wash solutions in pharmaceutical processes • WFI / PW applications • CIP media • Buffer and process solutions • Biotechnology • GMP production systems • Sterile liquid processes Documentation – fully available and structured Comprehensive, project-specific quality and manufacturing documentation included, such as: • EU declaration of conformity and warranties • Reports and EU component verifications • Assembly documents • Component drawings • TÜV certificate with acceptance report • Nameplate documentation • TÜV design review and certification • Welder lists, welding procedure qualifications, samples • Analysis certificates for welding filler material • Analysis certificates for shielding gas • Manufacturer qualification certificate • Non-destructive testing (NDT) reports • Material certificates (3.1) • Calibration certificates • Internal pressure test report • Dimensional accuracy check • Surface roughness report • Surface treatment report Rcjdpfjykkivsx Ahcef • Operating and maintenance manuals (unit) • Operating and maintenance manuals (components) • FAT documentation (Factory Acceptance Test) Complete documentation package available digitally. Special Feature This is not a standard tank, but a premium, custom-built unit in genuine pharmaceutical quality with certified pressure design, documented manufacture, and full PED compliance including TÜV acceptance. The heavy-duty construction, large connections, and CIP integration make this vessel ideal for demanding GMP applications.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 1,500 l, Equipment: documentation/manual, BRINOX 1,500 L Process Vessel – 1.4435 – Double Jacket – PED Module G – TÜV – FAT – 2020 – Like New Manufacturer: BRINOX d.o.o. Tag No.: BH6726-BH1001 Type: SVMBBI-1500 Year of Manufacture: 2020 Serial No.: 1003458 Equipment No.: 20051401 CE Marking: CE 0036 Condition: Like new / unused Empty weight: 866 kg TECHNICAL DATA Product type: Main filling vessel / process vessel Redpeykuhiefx Ahcscf Design: cylindrical with dished ends Working volume: 1,500 liters Total volume: 1,785 liters Product-contact material: 1.4435 Jacket material: stainless steel (double jacket design) Max. allowable pressure (PS) vessel: -1 / +3 bar Test pressure (PT): 5.4 bar Max. allowable temperature (TS): -10 °C / +150 °C Pressure vessel in accordance with PED 2014/68/EU Module: G Fluid group: 1 SURFACE & EXECUTION Internal surface: high-gloss polished, pharmaceutical design Product-contact areas made of 1.4435 Weld seams finely ground Pharmaceutical CIP-capable design EQUIPMENT • Double jacket for heating/cooling • Large manway with clamp closures • Multiple instrument and process nozzles • Pressure sensor / temperature connections • Bottom outlet • CIP/spray ball connections • Various blank flanges • Insulated media connections on jacket • FDA-compliant seals CONDITION • Never used in production • Stock item • Interior absolutely like new • No corrosion • No signs of use • Immediately available DOCUMENTATION – complete • EU Declaration of Conformity • TÜV acceptance documents • PED Module G documentation • Material certificates 3.1 • Pressure test report (PT 5.4 bar) • Technical drawings • FAT documentation • Operating manual SPECIAL FEATURE Large-volume BRINOX main filling vessel, 1,500 L in 1.4435, PED Category IV Module G, CE 0036, with complete documentation, pharmaceutical-grade surface finish, and pressure test at 5.4 bar. Project quality for sterile applications – immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 3,500 l, Equipment: documentation/manual, BRINOX 3,500 L Batch Tank – 1.4435 – Double Jacket – PED Module G – TÜV SÜD – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMBHI-3500 Tag No.: BH6770-BH1001 Serial number: 1003460 Year of manufacture: 2020 Condition: As new / unused BH6770-BH1001 Package 28 Redpfxoylng Ue Ahcscf TECHNICAL DATA Product type: Batch tank / pressure vessel Working volume: 3,500 liters Total volume: 4,304 liters Jacket volume: 202 liters Empty weight: 1,958 kg Product contact material: 1.4435 Jacket: 1.4404 CE marking: CE 0036 Permissible vessel pressure PS: -1 / +3 bar Test pressure vessel PT: 5.6 bar Permissible jacket pressure PS: -1 / +6 bar Test pressure jacket PT: 10.8 bar Permissible temperature TS: -10 °C to +150 °C Fluid group: 2 Design according to AD 2000 code Pressure vessel according to PED 2014/68/EU Category III Module G – Individual inspection Notified body: TÜV SÜD Industrie Service GmbH (ID number 0036) TÜV approval including final inspection and pressure test, fully documented. FAT – Factory Acceptance Test The vessel was fully FAT tested and approved at the factory. Tests carried out, among others: • Pressure test per PED • Visual inspection of all weld seams • Non-destructive tests (RT, PT according to test plan) • Dimensional and drawing comparison (as-built) • Internal surface roughness measurement (Ra ≤ 0.8 µm) • Calibration test of manometers • Marking verification • Complete documentation review Full FAT protocols available. DESIGN • Cylindrical, horizontal vessel • Double jacket with half-pipe system • Internally electropolished and passivated • High-gloss product contact surface • Pharmaceutical-grade welds • Manway DN 500 • Powder/product inlet DN 300 • CIP connections • Safety valve • Pressure and temperature connections • Agitator connection • Heavy-duty trunnion supports • Lifting lugs DOCUMENTATION – complete and structured Extensive project-specific quality and manufacturing documentation available, including: • EU Declaration of Conformity and guarantee certificates • TÜV certificate with acceptance report (Module G) • TÜV design review and certification • Material certificates 3.1 • Welder lists and welding procedure qualification records (WPQR/WPS) • Non-destructive test reports (RT, PT, etc.) • Analysis certificates for welding filler materials and gas • Company qualification certificate • Roughness protocol • Surface treatment report • Dimensional accuracy test report • Internal pressure test report • Calibration certificates • Reports and EU conformity of installed components • Parts list compilation • Detail drawings • Operating and maintenance manuals Complete digital documentation package available. CONDITION • Never used in production • Stock item • Interior surface absolutely as new • No corrosion • No signs of use • Industrial new condition • Immediately available SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP production plants • Biotechnological applications SPECIAL FEATURES High-quality BRINOX pharmaceutical fabrication with complete PED Module G individual approval by TÜV SÜD, CE 0036 marking, and fully documented FAT inspection. Not a standard tank – this is audited project quality with comprehensive GMP-compliant documentation.

Condition: used, 2 oil-free screw compressors for the production of sterile compressed air. Of these: - Compressor 1 (year of manufacture 2006): frequency-controlled with built-in dryer - Compressor 2 (year of manufacture 1992): with downstream adsorption dryer (Atlas Copco, 2003) Redezkfw Topfx Ahcecf Additional title: Compressed air generation with screw compressors; manufactured between 1992-2006 Capacity compressor 1: 5.952 m³/min, with a final pressure of 8.4 bar Capacity compressor 2: 4,982 m³/min, with a final pressure of 8.0 bar Features: 2 screw compressor (one of which has a built-in dryer and variable-speed drive, and one with a separate dryer)

Condition: new, Year of construction: 2020, functionality: fully functional, machine/vehicle number: BH6721-BH1001, tank capacity: 1,000 l, Equipment: documentation/manual, BRINOX 1,000 L Pre-Filling Tank – 1.4435 – Double Jacketed – PED Module G – TÜV SÜD – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMBBl-1000 Tag No.: BH6721-BH1001 Serial No.: 1003453 Year of Manufacture: 2020 Condition: As new / unused TECHNICAL DATA Product type: Pre-filling tank / process vessel Nominal volume: 1,000 liters Total volume: 1,400 liters Empty weight: 762 kg Product-contact material: 1.4435 (AISI 316L pharmaceutical grade) CE Marking: CE 0036 Permissible pressure PS: -1 / +3 bar Test pressure PT: 5.4 bar Permissible temperature TS: -10 °C to +150 °C Fluid group: 1 Design according to AD 2000 code Pressure vessel in accordance with PED 2014/68/EU Category IV Module G – Individual inspection Notified Body: TÜV SÜD Industrie Service GmbH (ID No. 0036) TÜV acceptance including final inspection and pressure test fully documented. FAT – Factory Acceptance Test The vessel underwent full FAT testing and approval at the manufacturer’s site. Tests carried out include: • Pressure test in accordance with PED • Visual inspection of all weld seams • Non-destructive testing (RT, PT as per test plan) • Dimensional and drawing check (as-built) • Internal roughness measurement (Ra ≤ 0.8 µm) • Calibration test of pressure gauges • Verification of markings • Complete documentation review FAT protocols fully available. DESIGN FEATURES • Cylindrical, horizontal tank • Double jacket for heating/cooling • Internally electropolished and passivated • High-gloss product contact surface • Pharmaceutical-grade weld seams • Manhole DN 500 • CIP connections • Safety valve • Pressure gauge • Bottom diaphragm valve • Agitator port (DN 200) • Multiple spare ports • Heavy-duty trunnion/pivot bearing • Transport and lifting devices DOCUMENTATION – fully complete and well structured Comprehensive, project-specific quality and manufacturing documentation available, including: • EU Declaration of Conformity and warranty certificates • TÜV certificate with acceptance report (Module G) • TÜV design test and certification • 3.1 material certificates • Welder lists and welding procedure qualifications (WPQR/WPS) • Non-destructive testing reports (RT, PT, etc.) • Analysis certificates for welding consumables and gases • Company qualification certificate • Roughness protocol • Surface treatment report • Dimensional accuracy report • Internal pressure test report • Calibration certificates for pressure gauges Rcodpfx Asykpqrshcjf • Reports and EU conformity of installed components • Parts list assembly • Component drawings • Operating and maintenance manuals Complete digital documentation portfolio available. CONDITION • Never used in production • Stock item • Internal surface absolutely as new • No corrosion • No signs of use • As-new industrial condition • Immediately available SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Buffer and media preparation • Sterile liquid processes • GMP production plants • Biotechnological applications SPECIAL FEATURE High-quality BRINOX pharma-manufacturing with complete PED Module G individual acceptance by TÜV SÜD, CE 0036 marking, and full FAT test documentation. Not a standard tank, but a quality project vessel with comprehensive GMP-compliant documentation. Immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, Machine designation BRINOX Process System / CIP Skid Type CS6700 (CS6723) GMP CIP Process Skid 1.4435 Manufacturer BRINOX Process Systems Year of manufacture 2020 Technical Data Design as a stainless steel process skid in hygienic execution. Conductivity measurement 1–500 µS/cm, analog signal (AI), hygienic connection DN 50. Flow measurement 0–18,000 kg/h, analog signal (AI), connection DN 25, sterile flange DIN 11864-2A. Pressure measuring points −1 to 9 bar and −1 to 15 bar, analog signal (AI), hygienic connections DN 50 or ½", e.g. DIN EN ISO 228. Temperature measuring points −50 °C to +200 °C, analog signal (AI), connection DN 32, welded according to DIN 11866/A. Limit level sensors, digital (DI), hygienic connection DN 50. Multiple position feedbacks with IO-Link / digital. Pneumatically actuated on/off valves (DO) in stainless steel hygienic design. Product-contact materials according to EN 1.4435 / 1.4404 (AISI 316L). Documented surface roughness of product-contact surfaces Ra approx. 0.3–0.4 µm. Application Hygienic CIP and process plant for pharmaceutical and biotechnological applications. Suitable for cleaning process lines and vessels under GMP conditions. Construction Welded stainless steel skid with orbital welded piping. Hygienic clamp and sterile connections. Fully instrumented with flow, pressure, temperature, and conductivity measurement. Pneumatic valve technology with digital feedback. Components from renowned manufacturers such as Endress+Hauser, Gemü, Samson, SICK, and others. Clean, GMP-compliant execution. Condition New. Original packaging. Unused. Never installed or commissioned. FAT / Documentation Status Fully documented Factory Acceptance Test carried out. Layout drawing inspection documented. Maintenance and calibration accessibility check documented. Surface roughness test documented. Leak test documented. Sensor calibration documented. Welding documentation fully verified. Complete Documentation List FAT plan and FAT report. P&I diagram. Layout drawings. Material lists for metals and polymers. Material certificates 3.1. WPQR, WPS, welder qualifications. Welding protocols and isometrics. Calibration certificates for measuring instruments. Surface roughness measurement protocols. Leak test protocols. EU declarations of conformity for installed components. Operating documentation. Special Features GMP-compliant, fully documented manufacturing. Rsdeyl H Svepfx Ahcecf High-quality instrumentation. Very low documented roughness values. Immediately available. Ideal for pharmaceutical, biotech, or contract manufacturers with high documentation requirements.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 1,500 l, Equipment: documentation/manual, BRINOX 1,500 L Main Precipitation Vessel – 316L – Double Jacket – PED Module G – FAT 2020 – As New Manufacturer: BRINOX d.o.o. Type: SVMBI-1500 Tag No.: BH6724-BH1001 Package 22 Serial Number: 1003457 Year of Manufacture: 2020 Condition: As new / unused CE Marking: CE 0036 TECHNICAL DATA Product Type: Main precipitation vessel / process vessel Nominal Volume: 1,500 liters Total Volume: 1,785 liters Empty Weight: approx. 866 kg Product-contact Material: 1.4435 (AISI 316L pharmaceutical grade) Jacket Material: Stainless steel Operating Pressure (Vessel): –1 / +3 bar Test Pressure (Vessel): 5.4 bar Operating Pressure (Jacket): as per design Temperature Range: –10 °C to +150 °C Pressure Vessel in accordance with PED 2014/68/EU Module G – Individual inspection Rcsdpfx Ahjykn Iijcjf Approval by notified body 0036 FAT – Factory Acceptance Test (08/2020) The vessel underwent a complete documented FAT at the BRINOX plant. Tests performed included: • Delta ferrite test of weld seams (conforming, no deviations) • Surface roughness check (Ra internal ≤ 0.8 µm, conforming) • Visual inspection of all product-contact surfaces • Pressure test as per specification • Documentation review • GMP deviation management (only non-critical points, fully resolved) • Measuring instruments with valid calibration certificates DESIGN • Double jacket for heating/cooling • Horizontal design • High-grade pharmaceutical finish • Fully constructed from 316L stainless steel in product-contact areas • Mirror-polished internal surface • GMP-compliant, documented weld seams • Large manway with swing cover • Multiple clamp and flange connections • Spray ball / CIP connections • Prepared for instrumentation (pressure, temperature, sensors) • Insulated jacket with connections • Heavy-duty flange base • Lifting lugs and transportation version • Project-specific build for CSL Behring (Project SPHINX) CONDITION • Never in productive use • Direct from project surplus • Absolutely as-new interior • No corrosion • No signs of use • Industrial as-new condition • Immediately available DOCUMENTATION Complete project-related quality and manufacturing documentation available, including: • EU Declaration of Conformity • TÜV inspection documents • PED Module G documentation • 3.1 material certificates • Welding documentation (WPS/WPQR) • Delta ferrite test protocols • Roughness measurement protocols • Calibration certificates for measuring instruments • GMP deviation protocols • Fully signed FAT protocols • Operating and maintenance manuals All documentation is complete and well-structured. • Pharmaceutical active substance processes • Precipitation and reaction processes • Buffer and solution preparation • Sterile liquid processes • Biotechnology • GMP production facilities • Ultra-pure media SPECIAL REMARKS This is a high-quality BRINOX process vessel in true pharmaceutical project quality, built for CSL Behring, with full PED Module G individual inspection, FAT 2020 documentation, and comprehensive GMP documentation. Not a standard tank, but certified project quality for sterile applications. Immediately available.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 1,500 l, Equipment: documentation/manual, BRINOX 1,500 L Process Vessel – 1.4435 – Jacketed – PED Module G – TÜV – FAT – 2020 – As New Manufacturer: BRINOX d.o.o. Tag No.: BH6722-BH1001 Year of manufacture: 2020 Condition: As new / unused CE Marking: CE 0036 TECHNICAL DATA Product type: Main/process vessel Design: Cylindrical with dished ends Working volume: 94 – 1,500 liters Empty weight: 866 kg Product contact material: 1.4435 Jacket material: 1.4307 Insulation: yes Rcjdeykuc Topfx Ahcsf Operating pressure (vessel): -1 / +3 barg Permissible pressure (PS): -1 / +3 barg Test pressure (PT): 5.4 bar Permissible temperature (TS): -10 °C / +150 °C Date of pressure test: 2020/04 Pressure vessel according to PED 2014/68/EU Category IV Assessment procedure: Module G Notified body: TÜV SÜD Industrie Service GmbH Design code: AD 2000 SURFACES & WELDS Internal surface: Electropolished and passivated Pharmaceutical grade External surface: Industrial ground finish NDT / Inspections: RT (radiographic testing) PT (penetrant testing) Pressure testing documented 2020 EQUIPMENT • Double jacket for heating/cooling • Large frontal manway • Multiple process nozzles • CIP connections • Temperature and pressure ports • Safety fittings • Agitator mount • FDA-compliant seals • Complete piping module CONDITION • Never used in production • Stock item • Internal surface absolutely as new • No corrosion • No signs of use • Available immediately DOCUMENTATION – fully available • EU Declaration of Conformity • TÜV certificates and inspection reports • PED Module G documentation • Material certificates 3.1 (EN 10204) • Welding logs • NDT reports (RT / PT) • 2020 pressure test report • Surface reports • Detail and assembly drawings • FAT documents • Operating and maintenance manuals SPECIAL FEATURE BRINOX pharma process vessel in 1.4435 with electropolished internal surface, AD2000 design, PED Category IV Module G, full TÜV inspection 2020, and complete technical documentation. Project quality for sterile applications – immediately available.

Condition: used, This listing is for a Pall Allegro 50 L Standard Mixer and Weigh Platform. The unit is in full working condition and is ready for immediate release. The Pall Allegro 50 L Standard Mixer and Weigh Platform is a robust and versatile solution designed for single-use bioprocessing applications in the pharmaceutical and biotechnology industries. Engineered for consistent mixing performance, this system supports critical upstream and downstream operations including buffer preparation, media mixing, and formulation processes. This platform integrates high-precision weighing functionality with a reliable mixing system, offering enhanced process control in a compact, easy-to-clean stainless steel frame. Its compatibility with Pall Allegro single-use mixers ensures operational flexibility and sterility assurance across various applications. Key Features Integrated Design – Combines mixing and weighing in one streamlined system. Single-Use Compatible – Fully compatible with Pall Allegro 2D mixer bags. High Accuracy Weighing – Precision load cells for reliable mass control and batch documentation. User-Friendly Interface – Easy-to-use control panel with adjustable speed and mixing profiles. Hygienic Construction – Stainless steel frame with smooth surfaces for GMP compliance. Scalable Solution – Ideal for pilot-scale to small-scale commercial production. Technical Specifications Model: Allegro 50 L Standard Mixer & Weigh Platform Mixing Volume: Up to 50 liters Mixer Type: Magnetically driven impeller Platform Material: 304 Stainless Steel Weight Capacity: Up to 100 kg Dimensions (approx.): 600 mm x 600 mm x 1100 mm Power Supply: 100–240 V AC / 50–60 Hz Control System: Integrated touch screen interface Manufacturer: Pall Corporation Applications Biopharmaceutical Manufacturing – Media and buffer prep, formulation, and hold steps. Clinical Manufacturing – Flexible use in small-scale GMP operations. Vaccine Production – Sterile formulation and component mixing. Rodpsxl Dpdsfx Ahcecf Gene & Cell Therapy – Supports sterile, closed-system processing. Process Development Labs – Ideal for scaling up single-use technologies. Benefits Sterile Processing – Supports single-use bags to minimize contamination risk. Compact Footprint – Fits easily into lab and production environments. Accurate Dosing – Integrated weigh system for precise process control. Reduced Cleaning Time – No need for CIP/SIP due to disposable mixer bags. Pall Quality – Developed by a trusted leader in bioprocessing technologies.

Condition: ready for operation (used), Engineered for high efficiency, the Steris VHP-100R Desiccant Regeneration System, Model RG120 regenerates desiccants used in vaporized hydrogen peroxide (VHP) sterilization, ensuring consistent and reliable moisture control. The RG120 is designed to maintain optimal performance of your VHP sterilization equipment, enhancing overall process efficiency and efficacy. Its robust construction, user-friendly interface, and advanced regeneration technology make the Steris VHP-100R Desiccant Regeneration System an essential component for any facility relying on VHP sterilization for critical applications. Good working condition. Please check out our other listings as well. Redew Rg Etopfx Ahcscf

Year of construction: 2025, condition: used, Merck Millipore Lynx ST Connector 1/2 in Fractional Triclover Code STC21THN01 Unused and in Original Packaging This is for 1 Unit although 50+ in stock Expiry Date: 31st August 2026 Sterilized fluid transfer systems containing tubing, connectors, clamps, valves, and disconnectors provide a critical link between disposable fluid paths and the various steps in your aseptic process, whether that is plastic-to-stainless or plastic-to-plastic. We offer three types of connectors and a crimping tool for sterile disconnection. We also can configure standard single-use assemblies with common types of commercially available tubing, such as platinum-cured silicone and C-Flex® 374 thermoplastic elastomer. Reliable and easy to use, Lynx® connectors feature unique designs that enable fluid transfer and maintain sterility. Lynx® connectors are available separately or as part of a complete assembly Redpoxv Afrjfx Ahcscf

Condition: used, operating hours: 1,800 h, Used Bottling Line for champagne, sparkling and still wine 4000 bph Product Compatibility and Filling Technology This bottling line processes still wine, sparkling wine, and champagne with high efficiency. Specifically, it handles only glass bottles and uses an isobaric filling system, which ensures precise control when filling pressurized liquids, such as sparkling products. As a result, wineries that produce multiple wine types with different physical and chemical properties can rely on this line for consistent, adaptable operation. In other words, the system addresses diverse product demands without compromising output quality. Performance Output by Bottle Format Depending on the bottle format, the line delivers different outputs. It processes both 0.20l and 0,375l bottles at 4,500 bottles per hour. Meanwhile, it handles 0,75l bottles at 4,000 bottles per hour and 1.5l bottles at 2,000 bottles per hour. Therefore, this production speed suits medium-scale wineries that require flexibility while maintaining industrial performance. Commissioning, Runtime, and Immediate Availability Technicians installed the line in 2022. Since that time, it has operated for 1,800 hours and produced approximately 2,400,000 bottles. The system continues to run in production, which means it remains in good operational condition. Furthermore, its immediate availability offers an advantage to wineries needing rapid deployment. Because of this, buyers can integrate the equipment without significant downtime. Primary Bottling Block: Depalletizing, Rinsing, Filling, and Capping The process starts with a Duetti Packaging depalletizer, model M, which automatically feeds empty bottles into the system. Subsequently, the GAI monoblock, model 4033RES-HP-A01, performs rinsing, filling, and capping in a single integrated unit. The dual-stage rinser (water + gas) uses 16 grippers to sanitize bottles. A high-pressure electropneumatic filler with 24 valves carries out isobaric filling. Notably, the 3-head rotary corker applies straight corks, champagne-style mushroom corks, plastic closures, and aluminum screw caps. Moreover, the monoblock includes multi-format screws, motorized guide adjustments, dummy bottles for internal rinser sterilization, and a solenoid valve kit to switch between gas and cleaning liquid inputs. Altogether, this configuration provides high precision, minimal changeover time, and excellent bottle handling. CIP and Quality Control: Cleaning and Inspection Systems To maintain hygiene, the WIN&TECH CIP unit, model Win&Guard C 23.05, manages automatic cleaning via a steam-water heat exchanger and a three-stage filtration system across two independent circuits. Additionally, this system allows operators to sanitize the internal components between production runs without disassembly. At the same time, the CMP inspection unit, model CV-MUF108, performs continuous quality control. Rjdpewgw Dgofx Ahcjcf

Condition: used, machine/vehicle number: LC540, Used aseptic filling line Tetra Pak A3 FLEX V150 200S up to 7000 l/hThe Used aseptic filling line Tetra Pak A3 FLEX V150 200S up to 7000 l/h provides an advanced solution for the aseptic bottling of dairy products and fruit juices. Consequently, this line fills 200 ml Slim Brick containers, ensuring high production efficiency and maintaining the sterility of the product throughout the entire packaging process.Line Features of the Used aseptic filling line Tetra Pak A3 FLEXThe bottling line operates with a capacity of up to 7000 liters per hour, ensuring high standards of safety and quality. Furthermore, the aseptic system prevents bacterial contamination, making this solution ideal for packaging sensitive liquids. Additionally, the line includes a conveyor system that facilitates the smooth transfer of containers between different processing stages, ensuring an uninterrupted workflow.Machines Included in the LineTetra Pak A3 FLEX V150 200 ml Slim Filler (year 2006)The Used aseptic filling line Tetra Pak A3 FLEX relies on the Tetra Pak A3 FLEX filler, which aseptically fills 200 ml Slim containers. Moreover, this machine utilizes an advanced sterilization system to guarantee the microbiological safety of the packaged product. The filling process ensures precision, thereby minimizing waste and maintaining accurate dosing.Tetra Pak Straw Applicator 22 (year 2009)The Tetra Pak Straw Applicator 22 automatically affixes straws to 200 ml Brick containers. As a result, its integration into the production line enables precise and fast application, improving the product’s ergonomics for the end consumer.Flow Management and Buffering: Tetra Pak Accumulator ACHX30-0500-47M (year 2010)The ACHX30-0500-47M accumulator optimizes production flow by regulating container transport between different processing stages. In addition, this component ensures a continuous workflow, preventing interruptions and maintaining a consistent production rate even when downstream machinery operates at variable speeds.Tetra Pak Cardboard Packer 70 (year 2003)The Tetra Pak Cardboard Packer 70 packages Brick containers into transport cartons. Consequently, the automated system enables fast and efficient packaging, protecting units during transportation and facilitating distribution logistics.Aseptic Filling Process in the Used aseptic filling line Tetra Pak A3 FLEXThe entire system performs aseptic filling, a technology that maintains product sterility without requiring refrigeration. Specifically, the process sterilizes the container before filling, preventing bacterial contamination and ensuring an extended shelf life.Safety and ComplianceThe Used aseptic filling line Tetra Pak A3 FLEX incorporates advanced safety systems to protect both operators and the product during processing. Additionally, each machine complies with the sanitary and hygiene regulations required by the food industry, ensuring safe production in line with international standards.Conclusion of the Used aseptic filling line Tetra Pak A3 FLEXThis aseptic bottling line serves as an ideal solution for large-scale production of dairy products and fruit juices. Given its capacity of 7000 l/h, it delivers high levels of efficiency, quality, and safety. Moreover, the state-of-the-art Tetra Pak machinery ensures a reliable process, minimizing waste... Rcjdpfezfzh Rsx Ahcof

Condition: good (used), MMM Group Vakulab HL Medical Autoclave This listing is for the MMM Group Vakulab HL Medical Autoclave. The unit is in full working condition and is ready for immediate use. Overview The Vakulab HL autoclave from MM Group Medical is a high-performance, GMP-compliant sterilizer designed for the safe, reliable, and validated sterilization of laboratory instruments, equipment, and materials. Specifically engineered for use in pharmaceutical manufacturing, biotechnology facilities, and research laboratories, the Vakulab HL combines advanced vacuum-assisted steam sterilization with robust stainless steel construction to ensure consistent results in even the most demanding applications. Key Features inc Advanced Steam Sterilization, Pre- and Post-Vacuum Cycles: Ensures efficient steam penetration and rapid drying, Optimized Steam Distribution: Uniform sterilization across all load types Programmable Cycles: Fully adjustable parameters for different sterilization needs. GMP & Cleanroom Ready, Double-Door Pass-Through Design (optional): For installation between clean and non-clean areas, Stainless Steel Chamber & Piping: High-grade AISI 316L for corrosion resistance and hygienic operation, Integrated Monitoring: Real-time cycle control with full batch documentation capability. Operational Safety & Control User-Friendly HMI: Touchscreen interface for programming and monitoring, Automatic Door Operation: With safety interlocks to prevent accidental opening under pressure, Built-In Diagnostics: Self-check functions for preventive maintenance. Technical Specifications. The Vakulab HL is a vacuum-assisted steam sterilizer available in multiple chamber volumes, typically ranging from 300 to 1,000 liters. The sterilization process operates at temperatures between 121 °C and 134 °C, controlled via a PLC-based system with an intuitive touchscreen human-machine interface (HMI). steam, water, compressed air, and electricity. It is designed to meet EN 285, PED, ISO 9001, and GMP compliance requirements, and can be validated to ISO 17665 sterilization standards. Applications - Pharmaceutical Manufacturing: Sterilization of equipment, components, and containers, Biotechnology: Sterilization of fermentation vessels, culture media, and instruments, Research Laboratories: Sterilization of glassware, tools, and lab consumables, Hospitals & Clinical Settings: Safe sterilization of surgical instruments and textiles, System Components, High-grade stainless steel chamber with polished finish, Vacuum pump system for pre- and post-cycle air removal, Steam generation and distribution system, Control panel with PLC and HMI touchscreen, Integrated temperature and pressure sensors for validation. Quality & Compliance, Manufactured in accordance with GMP guidelines, Complies with EN 285 and ISO 17665 sterilization standards, Full FAT/SAT/IQ/OQ/PQ support for validation in regulated environments, Designed for integration into cleanroom and production facilities, Benefits - Consistent, Validated Sterilization for a wide range of load types. Rsdpfxoyifqvj Ahcocf

Condition: used, Sterilizable universal filter for sterilization filtration. Stationary sheet filter with square filter elements in a vertical row arrangement, hydraulic filter sheet pressure. Hydraulic control from built-in electrical control panel. Additional title: Sterilisation filter, years of manufacture 1979-2010 Capacity approx.: 750 hl/h Sheet filter - filtration area approx. 356 - 493m2 Operating pressure: 8 bar Rcodpfexbn N Hex Ahcef Power: 6 kW Voltage: 220/380 V Frequency: 50 Hz Length: 10100 mm Width: 1320 mm Height: 1750 mm Formats: Square filter elements Operation / Control: Vertical row arrangement Material: Stainless steel Position: Horizontal Base construction: Frame Features: Filter sheets; hydraulik filter plate compression; hose pump Layer patterns: Vertical row arrangement

Condition: used, Year of construction: 1992, Technical details: Rcsdpfxou Nz I Ts Ahcjf max. temperature: 120 °C internal diameter: 980 mm internal length : 2580 mm external diameter: 1500 mm external diameter : 2740 mm wall strength: ca. 6,5 mm content: ca. 2000 l weight: 1425 kg Autoclave tank It is possible that this autoclave were built for the process of steam sterilization (according to operating parameters) The operating overpressure of +2 bar per room probably refers to the execution of the steam sterilization process, not to the pressure resistance of the container. - Permissible operating temperature 120 °C *

Condition: new, Year of construction: 2025, We produce and install complete plants for water and juice , still or carbonated. The complete line consists of : bottle blowing machine, automated feeding PET , compact washing , filling and Rodju Nad Tepfx Ahcocf capping machine. Each capping machine has automated cap feeder and sterilization station for caps. We provide high productivity filters and CIP automated hygienisation station. As option we can add the carbonated station completed with chiller and heat exchange unit. After bottles are filled we install X ray machine for inspection, oven for increasing liquid temperature, water blowing machine to clean the bottles, labeling machine, date and lot machine, bottle case packing machine, palletising unit, stretch film machine to hold pallets.