Used Gmp Surelamplus-800Ds for sale (129)

Condition: new, Year of construction: 2025, The Hight Speed Mixer SPT-SHM series are used to mix dry powder for tablets and capsules and can be also used for wet granulation Hjdpfx Alsh Im D Tj Sjl (pre-stage to tablet and capsule powder). All product touching parts are made out of SS 316L steel. Others are out of SS 304. The machines are conform to GMP standards and CE certificated. The output of the machine depends on the product.

Condition: new, Year of construction: 2026, Automatical capsule filling machines SPT-Series ( S. Korea) are design for fully automatic filling of hard gelantine capsules size #00 - #4, (optional # 000, 5) with powder, granulate or pellets for pharmaceutical and food supplements production. The equipment is distinguished by its high quality, simple operation. The disc method of filling provides high dosing accuracy. The machines are equiped with sets of tools for 1 capsule size from #00 to 5 (optional #000,5). The machines are conform to GMP standards and CE certificat; SPT-Series guarantee the highest quality of production! The capsule filling machine SPT-FS80 for general scale production; According to GMP regulations; HMI system; Touch screen, PLC control system; 2 years warranty; Installation and service from Germany Number of capsule holder per segment - 10 psc/h; Max.production quantity of capsules - 80 000 psc/h; Weight of machine - 2 500 kg; Hsdpfx Alody Dyne Ssl Space consumption - 1320 x 1050 x 1970 mm

Condition: new, Year of construction: 2026, Automatical capsule filling machines SPT-Series (S. Korea) are design for fully automatic filling of hard gelantine capsules size #00 - #4, (optional # 000, 5) with powder, granulate or pellets for pharmaceutical and food supplements production. The equipment is distinguished by its high quality, simple operation. The disc method of filling provides high dosing accuracy. The machines are equiped with sets of tools for 1 capsule size from #00 to #000,5. The machines are conform to GMP standards and CE certificat; SPT-Series guarantee the highest quality of production! The capsule filling machine SPT-FH100 for general scale production; According to GMP regulations; Hodpfxsdy Dyws Al Sel HMI system; Touch screen, PLC control system; 2 years warranty; Installation and service from Germany Number of capsule holder per segment - 14 psc/h; Max.production quantityof capsules - 110 000 psc/h; Weight of machine - 2 500 kg; Space consumption - 1650 x 1650 x 2030 mm

Condition: new, Year of construction: 2026, Automatical capsule filling machines SPT-FL25 Series (S. Korea) are design for fully automatic filling of hard gelantine capsules size #00 - #4, (optional # 000, 5) with powder, granulate or pellets for pharmaceutical and food supplements production. The equipment is distinguished by its high quality, simple operation. The disc method of filling provides high dosing accuracy. Hsdjdy Dyfspfx Al Ssl The machines are equiped with sets of tools for 1 capsule size from #00 to 5 (optional #000,5). The machines are conform to GMP standards and CE certificat; SPT-Series guarantee the highest quality of production! The small capsule filling machine SPT-FL25 for R&D and small general scale production; According to GMP regulations; HMI system; Touch screen, PLC control system; 2 years warranty; Installation and service from Germany Number of capsule holder per segment - 3 psc/h; Max.production quantity of capsules - 25 000 psc/h (by 1 segment hole); 17 000 psc/h (by 2 segments hole), 8 500 psc/h (by 1 segment hole). Weight of machine -700 kg; Space consumption - 900 x 1100 x 1700 mm

Condition: new, Year of construction: 2026, Automatical capsule filling machines SPT-Series (S. Korea) are design for fully automatic filling of hard gelantine capsules size #00 - #4, (optional # 000, 5) with powder, granulate or pellets for pharmaceutical and food supplements production. The equipment is distinguished by its high quality, simple operation. The disc method of filling provides high dosing accuracy. The machines are equiped with sets of tools for 1 capsule size from #00 to #5. The machines are conform to GMP standards and CE certificat; SPT-Series guarantee the highest quality of production! The capsule filling machine SPT-FH150 for general scale production; According to GMP regulations; HMI system; Touch screen, PLC control system; 2 years warranty; Hsdpsdy Dyzefx Al Sol Installation and service from Germany Number of capsule holder per segment - 20 psc/h; Max.production quantityof capsules - 150 000 psc/h; Weight of machine - 2 500 kg; Space consumption - 1750 x 1750 x 2100 mm

Condition: used, Used Packo approximately 35L stainless steel vertical reactor. Unit measures approximately 380mm diameter x 520mm straight side. Unit has a welded dished bottom and bolted flat top. Internal rated -1/6 bar maximum allowable working pressure. External stainless steel jacket rated 6 bar maxiumum allowable working pressure. Unit has bottom entry Novaseptic GMP 50 hygenic magnetic coupled mixer driven by a 0.25kW motor. Unit includes a local control panel. Mounted on a mobile stainless steel trolley. Hjdpfx Aoyw S S Tol Sol Weight: Estimated: Kg250.0 Dimensions: 850mm X 1050mm

Year of construction: 2018, condition: used, This listing is for a Solaris Biotech Solution Jupiter 3.0 Fermentor. The unit is in full working condition and is ready for immediate release. The Solaris Biotech Solution Jupiter 3.0 Fermentor is a highly versatile and configurable bioreactor system, ideal for laboratory-scale applications. With advanced automation and robust design, it caters to a wide range of research and development needs, as well as small-scale production. Key Features: Autoclavable and Sterilizable Design: Ensures ease of cleaning, sterility, and reliable operation for contamination-free processes. Flexible Vessel Options: Available in various aspect ratios and thermoregulation designs, with total volumes ranging from 2.0 L to 10.0 L. Pressure Control: Handles pressures up to 1.6 bar in the 2 L and 4 L jacketed vessels, with continuous gas-in and gas-out flux. Innovative SCADA Software (LEONARDO 3.0): Provides automated management of fermentation and cultivation processes, ensuring precision and ease of operation. Parallel Management: Hjdpfoxxz T Hjx Al Sel Supports simultaneous operation of up to 24 units via a single HMI with a 24” display, streamlining complex workflows. Remote Access: Enables monitoring and control via PC, tablet, or smartphone, using QR code scanning or a dedicated web portal for remote convenience. Applications: Process Development and Optimization: Facilitates experimentation and optimization of bioprocesses for scale-up and scale-down studies. Education and Research: Suitable for educational purposes and basic research in bioprocessing. Small-Scale Production: Supports small-batch manufacturing and pilot-scale processes. Benefits: Cost-Effective Performance: Combines advanced features with affordability for laboratory and production environments. High Level of Automation: Simplifies management of fermentation and cultivation with LEONARDO 3.0 software, reducing operator workload. Versatility and Configurability: Adaptable to a wide variety of applications, ensuring compliance with validated GMP regulations. Technical Specifications: Material: VALOX resin (external) and silicone (internal) Autoclavable: 121-133°C for up to 30 minutes Residual Volume: 0.04 mL Flow Rate: 65 mL/min

Year of construction: 2002, condition: used, This listing is for a Lancer Washer Infeed Type 1600 PCM DPSS The unit is in full working condition and is ready for immediate release. Lancer 1600 PCM Stainless Steel Washer Overview Hedpfxoxhfkus Al Sjl The Lancer Washer Infeed Type 1600 PCM DPSS is a superior pharmaceutical production washer designed to exceed all GMP requirements Ehret Technologies – Trio-Tech International. This industrial-grade washing system is specifically engineered for pharmaceutical and laboratory applications where stringent cleaning standards are essential. Key Features Designed to provide an adequate cleaning process using mechanical, thermal and chemical cleaning properties ETO Sterilizer - Fully Automatic ETO Sterilizer, Hospital Sterilizer Manufacturer Multi-level washing capabilities for maximum efficiency GMP (Good Manufacturing Practice) compliant design Pharmaceutical-grade construction and validation Chamber Specifications Internal chamber dimensions: 33 5/8"H × 27 3/4"D × 27 3/4"W ETO Sterilizer - Fully Automatic ETO Sterilizer, Hospital Sterilizer Manufacturer Large capacity design for high-volume processing Multiple rack positions for flexibility Construction & Materials 316L Stainless Steel Construction: Pharmaceutical-grade stainless steel throughout for corrosion resistance and easy sanitization cGMP Compliant: Meets current Good Manufacturing Practice requirements Robust Design: Built for continuous industrial use in demanding environments Control System Microprocessor-controlled operation Multiple programmable wash cycles Process monitoring and documentation capabilities Applications Pharmaceutical manufacturing equipment cleaning Laboratory glassware and instrument washing Medical device processing Research facility applications Biotechnology equipment cleaning Technical Specifications Model: 1600 PCM (Pharmaceutical Cleaning Module) Construction: 316L Stainless Steel Compliance: cGMP, FDA regulations Operation: Automated wash/rinse/dry cycles Chemical Integration: Automated detergent and rinse aid dosing Validation: IQ/OQ/PQ documentation available Benefits Ensures consistent, validated cleaning results Reduces manual labour and contamination risk Meets strict pharmaceutical industry standards Large capacity increases throughput Automated operation improves efficiency and traceability This washer represents Lancer's commitment to providing pharmaceutical-grade cleaning solutions that meet the most demanding industry requirements for cleanliness, validation, and regulatory compliance.

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. Hodpfsyifqvsx Al Ssl

Condition: new, Year of construction: 2020, functionality: fully functional, Equipment: documentation/manual, Package 15 PP6715 – CS6715 Brinox LEP 11 – Pharma Chromatography and CIP System New – original packaging – Factory New Manufacturer: Brinox Model: LEP 11 Version: PP6715 with CIP System CS6715 Condition: New, unused, original packaging Hedpfxeyl Rqpe Al Ssl Description For sale is a high-quality pharmaceutical chromatography system Brinox LEP 11, consisting of the PP6715 control panel and the corresponding CS6715 CIP unit. The system is completely new, unused, and in the manufacturer's original condition. It was designed for industrial C1-INH chromatography and meets the highest GMP standards. Scope of Functions - Slurry transfer - Washing and elution processes - Transfer to pre-precipitation tanks - Gel disposal - Independent CIP loop Technical Features - Product-contacting components in stainless steel 1.4435 - Electropolished, Ra ≤ 0.8 µm - FDA-compliant sealing systems - CIP/SIP-capable - Operating pressure up to 6 bar - Temperature range up to 95°C - Fully drainable piping CIP Skid CS6715 - Stainless steel frame - Centrifugal pump - Shell-and-tube heat exchanger - Temperature control of cleaning media - Adjustable feed pressure The system is in factory-new condition with zero operating hours.

Year of construction: 2020, condition: new, functionality: fully functional, Equipment: documentation/manual, Package 14 PP6713 – CS6713 Brinox LEP 11 – GMP Chromatography System with CIP Skid New – unused – in original packaging Manufacturer: Brinox Model: LEP 11 Hsdjyl Rnnspfx Al Sel Version: PP6713 with CIP System CS6713 Condition: New – in original packaging – never installed Description Offered is a pharmaceutical chromatography system LEP 11, consisting of the chromatography panel PP6713 and the corresponding CIP skid CS6713. The system is completely new, unused, and remains in the manufacturer’s original condition. The unit was designed for GMP-grade protein purification as part of C1-INH chromatography. System Features Cleanroom panel for wall integration Transfer lines to sieve-bottom tanks Precipitation vessel connection Gel waste disposal line Complete utility/process piping Technical Specifications Design pressure: –0.9 to +6 bar Design temperature: +2 to +95 °C Electropolished surfaces Ra ≤ 0.8 µm Material: 1.4435 stainless steel Fully drainable GMP-compliant design CIP System CS6713 Stainless steel frame construction Centrifugal pump Shell-and-tube heat exchanger Conductivity, pressure, and temperature monitoring Adjustable CIP supply flow The system is brand new and has never been in operation.

Condition: used, This listing is for an ÄKTA ready™ Chromatography System Hedpoyitvpsfx Al Sel The unit is in full working condition and is ready for immediate release The ÄKTA ready™ Chromatography System is a single‑use liquid chromatography platform engineered for bioprocessing, process scale‑up, and GMP‑regulated manufacturing of biologics, including monoclonal antibodies, recombinant proteins, viral vectors, nucleic acids, and other sensitive therapeutic products. Key Characteristics - Single‑use disposable flow paths — eliminate the need for cleaning and cleaning validation between runs, reduce downtime, and minimize cross‑contamination risk. - Flexible operation — available in multiple configurations (isocratic, gradient, variable UV, extended) to match different purification needs. - Scalable platform — flow kits for low and high flow rates support a wide range of process volumes; systems scale from small‑batch purification to larger process requirements when paired with larger ÄKTA ready™ XL models. - Designed for GMP environments — extensive documentation and regulatory support help meet compliance demands in regulated biopharmaceutical production

Year of construction: 2026, condition: new, Rotary Tablet Press SPT-TP 400 with high speed production capacity. High speed production capacity; According to GMP Regulations; Touch screen, PLC control platform; HMI system; SPT-TP 400 Number of station (max.) D=30 B=36 BB=45 1 Max.Tablet output tab/h 125000 170 000 215 000 2 Max.Tablet dia. Round mm 13 16 25 Shaped mm 14 19 25 3 Max. tablet Thickness mm 8,5 4 Max. main compression force Ton 10 Hodpfjdy Dzrox Al Ssl 5 Max. Pre compression force Ton 2 6 Machine Dimension mm 1000 x 1230 x 2000

Year of construction: 2026, condition: new, Rotary Tablet Press SPT- TP 500 D with double sided press with 2 layer production. Double sided press; 2 Layer production; According to GMP regulations; Touch screen, PLC control plarform; HMI system; SPT-TP 500D Number of station (max.) D=41 B=49 BB=59 1 Max.Tablet output(double sided) tab/h 270 000 360 000 420 000 Hodpfxsdy Dz Ao Al Ssl Max.Tablet output 2 layer tab/h 90 000 115 000 140 000 2 Max.Tablet dia. Round mm 13 16 25 Shaped 14 19 25 3 Max. tablet Thickness mm 8,5 4 Max. main compression force Ton 10 6 Machine Dimension mm 1150 x 1550 x 1950

Year of construction: 2026, condition: new, Rotary tablet press SPT-TPL200 is the small rotary press for R&D and small scale production. According to GMP regulations; Touch screen, PLC control platform; Hodpfx Ajdy Dziel Sol HMI system; Description SPT-TPL 200 Number of station (max.) D=13 B=16 BB=19 1 Max.Tablet output tab/h 46 000 57 000 68 000 2 Max.Tablet dia. Round mm 25 16 13 Shaped mm 25 19 14 3 Max. tablet Thickness mm 8,5 4 Max. main compression force Ton 5 5 Max. Pre compression force Ton 1 6 Machine Dimension mm 600 x 1106 x 1705

Condition: new, Year of construction: 2020, functionality: fully functional, Equipment: documentation/manual, Brinox LEP 11 – Pharmaceutical Chromatography System with CIP Unit New, unused, original packaging Manufacturer: Brinox Model: LEP 11 Version: PP6711 with associated CIP unit CS6711 Condition: New – unused – original packaging (Factory New Condition) Description For sale is a Brinox LEP 11 pharmaceutical chromatography system, consisting of the chromatography panel PP6711 and the associated CIP unit CS6711. The system is completely new, unused, and in its original packaging. It was designed, manufactured, and delivered, but has never been installed or put into operation. This unit is designed for C1-INH chromatography and is used for controlled protein purification using sieve-bottom vessels in a GMP environment. Process Functions • Transfer of loaded QAE resin (slurry) • Washing and elution processes • Transfer of eluate to pre-precipitation vessel • Gel disposal via container station • Fully automatic CIP and SIP cleaning Technical Data • Fully CIP and SIP capable • Design pressure: –0.9 to +6 bar Hedpfx Aoyl Ndnjl Sol • Design temperature: +2°C to +95°C • Flow rate up to 10 m³/h • Adjustable slurry transfer 0.2 – 3 m³/h Design Features • Product-contact parts made of stainless steel 1.4435 • Electropolished Ra ≤ 0.8 µm • FDA and EU-compliant seals • Drainable construction • Cleanroom panel with tri-clamp connection points • Magnetically monitored transfer arcs • 0.2 µm vent filter CIP Unit CS6711 • Compact stainless steel skid • Centrifugal pump • Shell-and-tube heat exchanger • Adjustable operating pressure • GMP-compliant design The system is in factory-new condition and has never been used in production.

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 3,500 l, Equipment: documentation/manual, BRINOX 3,500 L Storage Tank – 1.4435 – Double Jacket – PED Module G – TÜV SÜD – FAT – 2020 – Like New Manufacturer: BRINOX d.o.o. Type: SVBBHI-3500 Tag No.: BH6772-BH1001 Package 30 Serial Number: 1003462 Year of Manufacture: 2020 Condition: Like new / unused TECHNICAL DATA Product Type: Storage / Process Tank Nominal Volume: 3,500 litres Total Volume: 4,082 litres Jacket Volume: 226 litres Empty Weight: approx. 1,760 kg Product-contacting Material: 1.4435 (AISI 316L pharmaceutical grade) Jacket Material: 1.4404 CE Marking: CE 0036 Hjdpfx Aoylnwyjl Ssl Permissible Pressure PS (Tank): -1 / +3 bar Permissible Pressure PS (Jacket): -1 / +6 bar Test Pressure PT (Tank): 5.6 bar Test Pressure PT (Jacket): 10.8 bar Permissible Temperature TS: -10 °C to +150 °C Fluid Group: 2 Designed in accordance with AD 2000 regulations Pressure vessel according to PED 2014/68/EU Category IV Module G – Individual Inspection Notified Body: TÜV SÜD Industrie Service GmbH (ID No. 0036) TÜV approval including design review, final inspection and pressure test fully documented. FAT – Factory Acceptance Test The vessel has been fully inspected and released by the manufacturer. Tests carried out include: • Pressure test as per PED • Design review by TÜV SÜD • Visual inspection of all weld seams • Non-destructive testing (RT, PT) • Dimensional and drawing check (as-built) • Review of material certificates • Calibration check of manometers • Verification of markings • Documentation review as per inspection checklist Full FAT and TÜV inspection reports available. EXECUTION • Cylindrical, horizontal storage tank • Double jacket for heating/cooling • High-quality pharmaceutical design • Manhole with round pressure closure • CIP pipework • J-pipe / internal piping • Sight glass DN80 • Multiple spare and process connections • Biocontrol flanges • Heavy-duty mounting blocks / trunnion design • Lifting lugs • Nameplate with complete PED marking DOCUMENTATION – complete and well-structured • EU declaration of conformity • TÜV certificate with inspection report (Module G) • TÜV design assessment and certification • 3.1 material certificates • Welder lists and work samples • Non-destructive test reports (RT, PT) • Dimensional inspection reports • Manometer calibration reports • Surface and production reports • Parts list • Detailed drawings (body, lid, CIP, J-pipe, etc.) • Operating and maintenance manuals Complete digital documentation folder available. CONDITION • Never put into operation • Was in storage • Interior surface 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 • Chemical media • GMP production facilities • Process and waste management plants SPECIAL FEATURE Premium BRINOX pharmaceutical-grade manufacture with full PED Module G individual inspection by TÜV SÜD, CE 0036 marking and documented FAT testing. Not a standard tank – certified project quality with comprehensive GMP-compliant documentation.

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 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 Hodpjylng Usfx Al Sel • 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, This listing is for an ÄKTA ready™ Chromatography System The unit is in full working condition and is ready for immediate release The ÄKTA ready™ Chromatography System is a single‑use liquid chromatography platform engineered for bioprocessing, process scale‑up, and GMP‑regulated manufacturing of biologics, including monoclonal antibodies, recombinant proteins, viral vectors, nucleic acids, and other sensitive therapeutic products. Key Characteristics - Single‑use disposable flow paths — eliminate the need for cleaning and cleaning validation between runs, reduce downtime, and minimize cross‑contamination risk. Hedpfx Aleyhhgaj Sel - Flexible operation — available in multiple configurations (isocratic, gradient, variable UV, extended) to match different purification needs. - Scalable platform — flow kits for low and high flow rates support a wide range of process volumes; systems scale from small‑batch purification to larger process requirements when paired with larger ÄKTA ready™ XL models. - Designed for GMP environments — extensive documentation and regulatory support help meet compliance demands in regulated biopharmaceutical production

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 Hjdjykqmzepfx Al Sel • Material certificates EN 10204 3.1 • WPS/WPQR and welders’ lists • NDT reports • Surface roughness protocols • 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, 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 • 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. Hodpfxeykpqre Al Sel 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, tank capacity: 30,000 l, Equipment: documentation/manual, BRINOX 30,000 L WWAS / Solution Tank – 316L – PED – FAT – Complete GMP Documentation – incl. Saddle Supports – 2020 – Like New Manufacturer: BRINOX d.o.o. Tag No.: LV6456-BH1001 Serial No.: 1003464 Year of Manufacture: 2020 Condition: Like new / unused Location: Europe LV6456-BH1001 Package 66 TECHNICAL DATA Product type: WWAS / solution tank / pharmaceutical process vessel Working volume: 30,000 liters Total volume: 33,213 liters Product contact material: Stainless steel 1.4404 (AISI 316L) Surface finish: Chemically pickled, passivated and cleaned Surface roughness: Ra < 1.6 µm Standards and guidelines: • PED 2014/68/EU compliant • CE marking available • GMP-compliant pharmaceutical design Pressure data: Min.: –0.14 bar(g) Max.: +0.5 bar(g) Test pressure: 0.72 bar(g) Temperature range: –20°C to +50°C Hydrostatic pressure test performed. FAT – Factory Acceptance Test Fully documented FAT carried out including: • Dimensional, visual, and identification inspection • Weld seam testing and NDT • Pressure test according to PED • Testing of all connections • Documentation and quality inspection FAT successfully completed. FAT report available. DESIGN / CONSTRUCTION • Horizontal pharmaceutical process vessel • Stainless steel 316L, pharmaceutical grade • Interior surface pickled and passivated • Hygienic, GMP-compliant construction Connections include: • Manway DN500 • Inlet DN100 • Outlet DN50 • Measuring, safety, and process connections Mechanical configuration: • Original BRINOX stainless steel saddle supports included • Heavy-duty design • Lifting points for crane handling present CONDITION • Absolutely as new • Never installed or used in production • Never filled with product • No corrosion or signs of use • Original industrial packaging available • Immediately available Saddle supports are also as new and included in delivery. DOCUMENTATION – fully available (GMP-compliant) Extensive manufacturer and project documentation including: • EU Declaration of Conformity and CE documentation • PED certificates • Material certificates EN 10204 – 3.1 • Welding documents (WPS/WPQR, welder lists) Hsdpfx Asykngfol Ssl • NDT inspection reports • FAT protocol and pressure test report • Roughness and surface protocols • Calibration certificates • Part drawings and parts lists • Operation and maintenance manuals Documentation fully available in digital form. TRANSPORT AND PACKAGING • Professional export packaging provided • Original industrial packaging • Crane handling possible without issues • Worldwide shipping possible SUITABLE FOR • Pharmaceutical industry • Biotechnology • WWAS, WFI, and PW systems • Sterile process solutions • GMP production plants SPECIAL FEATURE Project surplus from an international pharmaceutical new-build project with complete FAT, PED compliance, and GMP documentation. Large-capacity BRINOX 30,000 L pharma process vessel in as-new installation quality, incl. saddle supports – immediately available.

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 • Operating and maintenance manuals (unit) • Operating and maintenance manuals (components) Hjdpfxeykkivj Al Sol • 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: 3,200 l, Equipment: documentation/manual, BRINOX 3,200 L Solution Vessel – 316L – Double Jacket – TÜV / PED Module G – FAT – 2020 – As New Package 17 Manufacturer: BRINOX d.o.o. Tag No.: BH6762-BH1001 Year of manufacture: 2020 Condition: As new / unused TECHNICAL DATA Product type: Elution / Solution Vessel Volume: 3,200 liters Material: 1.4404 (AISI 316L) CE marking: available (CE 0036) Vessel pressure: Operating pressure: -1 / +3 bar Test pressure: As per TÜV inspection Jacket pressure (heating/cooling jacket): Operating pressure: -1 / +6 bar Test pressure: As per TÜV inspection Temperature range: -20 °C to +150 °C Pressure vessel in accordance with PED 2014/68/EU Module G – Single unit inspection Acceptance by notified body (identification number 0036) FAT – Factory Acceptance Test The vessel was tested as part of a documented FAT. The tests included, among others: • Verification of welding documentation • Visual inspection of weld seams • Leak testing • Pressure testing • Surface roughness inspection • Sensor calibration check • Layout and dimensional inspection • Documentation review The complete FAT report including test protocols is available. SPECIFICATION • Double jacket for heating/cooling • Entirely made of stainless steel 316L • High-gloss polished internal surface • Pharmaceutical-grade weld seams • CIP/SIP-capable connections • Multiple manways / inspection openings • Clamp and flange connections • Instrumentation ready (pressure, temperature, sensors) • Heavy-duty project construction • Lifting lugs for crane handling CONDITION • Never used in production • Surplus stock from project overrun • Interior absolutely clean • No corrosion • No signs of use • As-new industrial condition • Immediately available DOCUMENTATION – complete and structured Comprehensive, project-specific quality and manufacturing documentation is available for the vessel, including: • EU Declaration of Conformity and warranty certificates • TÜV certificate with acceptance report • TÜV design inspection and certification • Material certificates (3.1) • Welder lists and welding procedure qualification records (WPQR/WPS) • Non-destructive testing reports (NDT) • Analysis certificates for welding consumables and shielding gas • Surface roughness protocol • Surface treatment report • Dimensional accuracy check • Internal pressure test • Calibration certificates • Assembly records • Drawings (detail and overall) • Operating and maintenance manuals Complete documentation file available digitally. SUITABLE FOR • Pharmaceutical solutions • WFI / PW systems • Elution / buffer preparation • Sterile liquid processes • Biotechnology • GMP production plants • CIP media SPECIAL FEATURE This is not a standard tank, but a premium BRINOX project build in true pharmaceutical quality with verified pressure design, full PED conformity (Module G), documented FAT testing, and comprehensive quality documentation. Project-level quality for sterile applications – available immediately. Hodpfx Aleykkhro Sel

Condition: new, Year of construction: 2020, functionality: fully functional, tank capacity: 3,200 l, Equipment: documentation/manual, BRINOX 3,200 L Solution Tank – 316L – Double Jacket – TÜV / PED Module G – FAT – 2020 – Like New Manufacturer: BRINOX d.o.o. Tag No.: BH6761-BH1001 Serial Number: 1003446 Hjdpfjykkbxsx Al Sel Year of Manufacture: 2020 Condition: Like New / Unused Technical Data Product Type: ELUTION / Solution Tank Volume: 3,200 liters Empty Weight: 1,815 kg Material: 1.4404 (AISI 316L) CE Marking: CE 0036 Tank Pressure Operating Pressure: -1 / +3 bar Test Pressure: 4.6 bar Jacket Pressure (Heating/Cooling Jacket) Operating Pressure: -1 / +6 bar Test Pressure: 10.8 bar Temperature Range: -20°C to +150°C Pressure vessel according to PED 2014/68/EU Module G – Single Inspection Notified Body: TÜV SÜD (Identification No. 0036) Permitted Number of Load Cycles: 7,300 / 5,475 at pressure fluctuation ranges of 3.3 / 4.5 bar TÜV / PED / FAT • EU Certificate of Conformity according to 2014/68/EU • Certificate No.: Z-EU-SI-LJU-20-08-2350154-14124056 • Inspection report available • Pressure test with water successfully completed • Approval by TÜV SÜD Industrie Service GmbH • Factory Acceptance Test (FAT) performed • Module G individual acceptance • Turn-Over Package (TOP) fully available Complete Documentation Available The complete technical documentation package is available, including: • EU Declaration of Conformity and warranty certificates • TÜV certificate with acceptance report • TÜV design review and certification • Nameplate documentation • Assembly drawings • Detailed drawings • Welder lists and weld process qualifications • Work samples • Analysis certificates for welding consumables • Analysis certificates for shielding gases • Manufacturer qualification certificate • Non-destructive testing (NDT) reports • Material certificates (3.1) • Calibration certificates • Internal pressure test report • Dimensional accuracy check • Roughness protocol • Surface treatment report • Operating and maintenance manuals (equipment and components) The documentation scope meets project standards for pharmaceutical plants. Design Features • Double jacket for heating and cooling • Manufactured entirely from stainless steel 316L (1.4404) • High-gloss polished internal surface • Pharmaceutical-grade weld seams • CIP/SIP-capable connections • Multiple manholes / inspection openings • Clamp and flange connections • Instrumentation pre-installed (pressure, temperature, sensors) • Heavy-duty project design • Lifting lugs for crane handling • PED-compliant pressure design Condition • Never used in production • Stock from project surplus • Absolutely clean interior • No corrosion • No signs of use • As-new industrial condition • Immediately available Suitable for • Pharmaceutical solutions • WFI / PW systems • Elution / buffer preparation • Sterile liquid processes • Biotechnology • GMP production plants • CIP media Special Feature This is not a standard tank, but a high-quality BRINOX project-built vessel in genuine pharmaceutical quality featuring: • PED Module G individual inspection • TÜV SÜD approval • FAT performed • Complete welding, material, and inspection documentation • Documented surface treatment • 316L construction for sterile applications Project quality for demanding GMP applications – immediately available.