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VX-75 Vertical Laboratory

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VX-75 Vertical Laboratory
Systec Sterilization & Disinfection

VX-75 Vertical Laboratory

Where Large-Volume Lab Sterilization Meets Full Cycle Traceability

The Systec VX-75 is a CE-certified Class B vertical autoclave sterilizer offering 75-litre chamber capacity, fractionated pre-vacuum steam sterilization, and full automated cycle documentation. Designed for laboratory, pharmaceutical, research, and clinical environments requiring large-volume validated instrument and media sterilization, it meets EN 13060 and ISO standards for regulated scientific and medical settings.

Sections
Autoclave
Categories
Sterilization & Disinfection
Condition
Good
Seller Type
Professional Seller
CE & ISO Certified
Global Shipping
Supplier: Medigear
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The Systec VX-75 is a CE-certified Class B vertical autoclave sterilizer engineered for high-throughput sterilization in laboratory, pharmaceutical, research, and clinical environments where large-volume validated decontamination is required. Manufactured by Systec, a specialist in laboratory sterilization technology, the VX-75 combines a 75-litre vertical chamber with fractionated pre-vacuum steam sterilization to deliver validated Class B decontamination of all load categories — including solid instruments, porous materials, wrapped loads, and liquid media — across a single configurable platform.

The fractionated pre-vacuum cycle removes residual air from the chamber in multiple stages before the introduction of pressurised saturated steam, ensuring thorough and uniform steam penetration throughout the entire chamber volume and across complex load geometries. This is particularly critical for laboratory environments sterilizing mixed loads comprising instruments, porous packaging, and sealed liquid containers, where partial air removal would compromise sterilization efficacy.

The vertical chamber design maximises usable volume while minimising the unit's floor footprint, making the VX-75 well suited to laboratory environments where bench and floor space is shared across multiple instruments. The stainless steel chamber provides corrosion resistance and durability across repeated high-temperature cycles throughout the operational lifespan of the unit.

Automated cycle documentation records temperature, pressure, and duration data for every sterilization run, generating a full traceable record that satisfies the documentation requirements of pharmaceutical GMP environments, medical device regulatory frameworks, and laboratory quality management systems. Medigear.uk supplies the Systec VX-75 with full CE certification documentation, supporting institutional procurement, tender submissions, and distributor supply requirements.

Pharmaceutical and Biotech Laboratory Sterilization

Pharmaceutical and biotechnology laboratories require validated, documented sterilization for instruments, media, glassware, and packaging as a core GMP compliance requirement. The VX-75 provides fractionated pre-vacuum Class B sterilization with automated cycle documentation, supporting lot traceability and validation requirements of pharmaceutical environments regulated under MHRA, EMA, and equivalent frameworks.

University and Research Laboratory Instrument Sterilization

Research laboratories require large-volume sterilization for mixed loads including instruments, culture media, porous packaging, and biological waste. The VX-75's 75-litre chamber and configurable cycle programming support diverse load types and throughput demands across life sciences, microbiology, and materials science research disciplines requiring high-volume validated sterilization.

Hospital Central Sterile Services and Instrument Reprocessing

Hospital sterile services requiring validated large-volume decontamination benefit from the VX-75's Class B sterilization capability and automated documentation. Cycle traceability supports infection control audit requirements and assists procurement teams managing formal tender and compliance documentation processes.

Medical Device Manufacturing and Quality Control

Medical device manufacturers operating under ISO 13485 require validated sterilization equipment with documented cycle outputs. The Systec VX-75 provides validated Class B performance and automated documentation supporting manufacturing quality management systems and regulatory submission requirements across production environments.

Veterinary Research and Diagnostic Laboratories

Veterinary research facilities routinely sterilize instruments, culture media, and laboratory equipment in volumes exceeding smaller benchtop autoclave capacity. The VX-75's 75-litre vertical chamber and fractionated pre-vacuum capability support the high-volume sterilization demands of veterinary research and diagnostic laboratory environments effectively.

For Hospitals, Research Institutions, and Healthcare Procurement

The Systec VX-75 carries CE marking and meets EN 13060 Class B and applicable ISO standards, providing the compliance documentation required for formal hospital tender submissions, research institution procurement, and healthcare regulatory frameworks. Its automated cycle documentation supports infection control audit requirements and GMP compliance frameworks. Medigear.uk provides full CE certification records and supports institutional and government procurement channels.

For Pharmaceutical, Biotech, and Research Facilities

The VX-75's fractionated pre-vacuum sterilization, 75-litre chamber capacity, and automated documentation output make it suitable for pharmaceutical GMP environments, biotech research laboratories, and regulated research facilities requiring validated sterilization with full lot traceability. Its configurable cycle programming supports the mixed load requirements of active research workflows without the need for multiple sterilization platforms. Medigear.uk can provide technical specifications, validation support documentation, and procurement assistance.

For Medical Equipment Distributors and Laboratory Equipment Suppliers

Large-volume validated laboratory autoclaves address consistent demand across pharmaceutical, biotech, university, hospital, and veterinary markets — a commercially resilient product category with strong procurement renewal cycles. The Systec VX-75's Class B performance, 75-litre capacity, and automated documentation position it competitively in the mid-to-premium laboratory sterilizer segment. Medigear.uk offers authorised supply access with full CE documentation and technical support infrastructure for distributors serving laboratory and healthcare equipment markets.

75-Litre Vertical Chamber for Large-Volume Laboratory Loads

The VX-75 provides a 75-litre stainless steel vertical chamber accommodating large mixed loads including instruments, glassware, porous packaging, and liquid media in a single run. The vertical design maximises volume relative to footprint, supporting laboratories managing multiple instruments in shared space.

Fractionated Pre-vacuum for Complete Steam Penetration

The multi-stage fractionated pre-vacuum process removes residual air before steam entry, eliminating pockets that prevent uniform sterilant penetration across complex load geometries — critical for laboratories sterilizing mixed loads of instruments, porous materials, and liquid containers.

EN 13060 Class B Validated Sterilization

The VX-75 meets EN 13060 Class B for steam sterilizers, validating complete sterilization of solid, porous, wrapped, and hollow instrument loads — supporting regulated pharmaceutical, medical device, and laboratory environments requiring documented compliance.

Automated Cycle Documentation for Regulatory Compliance

Every cycle generates an automatic record of temperature, pressure, and duration, producing a full traceable log per processed load — supporting GMP frameworks, infection control audit requirements, and quality management systems without manual recording.

CE Marking and ISO Regulatory Compliance

The Systec VX-75 carries CE marking conforming to applicable ISO standards for laboratory steam sterilizers. Full compliance documentation is available through Medigear.uk for institutional procurement, regulatory submissions, and tender requirements.

Configurable Cycle Programming for Mixed Load Types

Multiple programmable cycle configurations support solid instruments, liquid media, and porous loads within a single platform — reducing the need for separate sterilization equipment and supporting efficient throughput across diverse laboratory workflows.

The Systec VX-75 laboratory autoclave sterilizer delivers EN 13060-validated Class B fractionated pre-vacuum sterilization with a 75-litre vertical chamber and automated cycle documentation — providing the large-volume validated decontamination capability that pharmaceutical laboratories, research institutions, hospitals, and medical device manufacturers require for full regulatory compliance and consistent operational efficiency across all load types. Its vertical chamber design, configurable cycle programming, and full traceable documentation output make it a reliable and versatile sterilization platform for demanding laboratory and clinical environments of all types and scales. Contact Medigear.uk for product specifications, compliance documentation, procurement assistance, or expert consultation.

FAQ

Frequently Asked Questions

Everything buyers need to know about sourcing medical equipment through MediGear.

The Systec VX-75 has a 75-litre vertical stainless steel chamber, accommodating large and mixed laboratory loads including instruments, glassware, porous materials, and liquid media in a single sterilization run. This capacity makes it suitable for high-throughput laboratory environments requiring large-volume validated sterilization beyond the capability of standard benchtop autoclaves. Medigear.uk can provide full load configuration guidance on request.

The Systec VX-75 meets the EN 13060 Class B standard for steam sterilizers, validating complete sterilization of all load categories including solid, porous, wrapped, and both Type A and Type B hollow instruments. This validation supports deployment in regulated pharmaceutical, medical device, and laboratory environments where documented sterilization compliance is a regulatory requirement.

Fractionated pre-vacuum sterilization is a multi-stage air removal process that systematically evacuates residual air from the sterilization chamber in sequential pulses before the introduction of pressurised saturated steam. This ensures uniform steam penetration throughout the chamber volume and across complex load geometries including porous materials, wrapped instruments, and liquid containers — preventing the partial sterilization failures that can result from incomplete air removal in gravity-displacement cycles.

Yes. The Systec VX-75 is designed to sterilize liquid media including culture media, buffer solutions, and other laboratory liquids alongside solid instruments and porous loads within its configurable cycle programming. Specific cycle parameters for liquid loads are available from Medigear.uk to ensure correct temperature, pressure, and hold time settings for validated liquid media sterilization.

Every sterilization cycle on the Systec VX-75 automatically records temperature, pressure, and duration parameters for the full cycle run, generating a complete documentation record per load. This record supports the lot traceability requirements of pharmaceutical GMP environments, infection control audit frameworks, and laboratory quality management systems, reducing manual documentation workload and providing a reliable regulatory compliance record for every sterilized load.

The Systec VX-75 carries CE marking and is manufactured in conformity with applicable ISO standards for laboratory steam sterilizers and EN 13060 for Class B performance validation. Full certification documentation is available from Medigear.uk, supporting formal institutional procurement, regulatory submissions, and tender requirements for clinical and laboratory purchasing.

Yes. The Systec VX-75's fractionated pre-vacuum Class B sterilization, automated cycle documentation, and EN 13060 validation make it suitable for pharmaceutical manufacturing and research environments operating under GMP frameworks. Its documentation output supports lot traceability requirements, and its validated performance supports process validation documentation required by pharmaceutical regulatory frameworks. Medigear.uk can provide technical documentation to support GMP qualification activities.

The Systec VX-75 requires a stable laboratory floor space, appropriate electrical supply, and water connection. Installation is performed by trained service engineers and includes commissioning, initial cycle validation, and operator training. Annual preventive maintenance and performance revalidation are recommended per the manufacturer's service schedule. Medigear.uk can coordinate installation, commissioning, and AMC arrangements as part of the procurement process.