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GloveFAST Cyto Pharma – Cytotoxic Isolator

Overview

GloveFAST Cyto Pharma is a high-performance negative pressure cytotoxic isolator designed for the safe handling of hazardous drugs. Ideal for hospital pharmacies and aseptic compounding units, it ensures operator and environmental protection during chemotherapy preparation, cytotoxic reconstitution and toxic API development. With advanced HEPA filtration, ergonomic design and low noise output, it offers class-leading safety without compromising user comfort.

 

 

Product Details

Key Features

  • Suitable for preparation of cytotoxic drugs, CMRs and hazardous APIs
  • Class 2 negative pressure isolator with ISO 3 air cleanliness in the working area
  • Fully compliant with ISO 14644-1, ISO 14644-7, DIN 12980:2017, EN 1822 and EN 61010
  • Real unidirectional (laminar) airflow at 0.45 m/s; exhaust flow rate of 300 m³/h
  • Multiple HEPA H14 filters ensure containment and filtration at every stage
  • Quiet operation – noise levels as low as 48 dB(A)
  • ECS® microprocessor control system automatically compensates for pressure and airflow variations
  • Integrated digital display with continuous monitoring of velocity, temperature, pressure and filter status
  • Audio-visual alarms for out-of-range airflow, pressure failure, filter saturation and more
  • Ergonomic design with >480 mm legroom, 2000+ Lux lighting and sloped viewing window
  • Front glove ports (Ø300/250 mm) with neoprene gloves and CSM sleeves; easy glove/sleeve replacement system
  • Removable AISI 316L stainless steel work surface with spill retention
  • Transfer hatches with sliding trays and interlocked doors
  • Smooth, GMP-compliant interior surfaces for easy cleaning
  • Foot-switch operation for hands-free access to transfer hatches
  • IP66 electrical sockets (x2) included as standard
  • Bag-out filter system for safe disposal of contaminated filters

 

Common Applications

  • Chemotherapy compounding
  • Reconstitution of cytotoxic/lyophilised drugs
  • Handling antineoplastic drugs or CMR substances
  • Toxic substance development in pharmaceutical and chemical research

Compliance

  • ISO 14644-1 (Air Cleanliness)
  • ISO 14644-7 (Containment)
  • EN 1822 / IEST-RP-CC00 (Filtration)
  • EN 61010 (Electrical Safety)
  • DIN 12980:2017 (CMR Handling Safety)

Available Options & Accessories

  • Automatic pressure decay test system (ATV valve)
  • Electrical sliding doors for hatches
  • Inflatable gaskets for VHP decontamination
  • RemoteFAST remote support interface
  • Additional glove/sleeve test discs
  • H₂O₂ pipework integration for Steris, Bioquell, etc.
  • 19” cleanroom touchscreen
  • Compressed air, vacuum and nitrogen connections
  • Hanging rail, isokinetic probe, air sampler port, intercom, CCTV, and more
  • Fully stainless steel body and hatches (optional)
  • Bespoke configurations available, including integrated cytotoxic cabinet line

Construction Materials

  • Work surfaces: AISI 316L stainless steel
  • Side and back walls: AISI 304L stainless steel
  • Transfer hatch carcass: Epoxy-painted steel with Alesta® antimicrobial coating

 

Variants

Model Outer Dimensions (W x D x H, mm) Work Chamber (W x D x H, mm) Weight (kg) Noise Level (dB(A))
2-4-2 2510 x 870 x 2300 1192 x 580 x 740 550 ≤ 48
2-5-4 2815 x 870 x 2300 1497 x 580 x 740 580 ≤ 50
2-6-4 3120 x 870 x 2300 1802 x 580 x 740 620 ≤ 51

 

Pack Sizes / Ordering Info

  • Available in 3 sizes with either 2 or 4 glove ports
  • Custom versions on request
  • Please contact MSC for configuration support, delivery lead time and installation requirements

Customisation

  • Fully bespoke solutions available including:
    • H₂O₂ rapid gassing hatch
    • Integration with cytotoxic safety cabinet
    • DPTE port integration
    • 3-way hatch configurations
    • Extended monitoring and validation tools

 

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