Aseptic isolator CDC F
containmentfor cancer drugsfor cytotoxics

Aseptic isolator - CDC F - Envair - containment / for cancer drugs / for cytotoxics
Aseptic isolator - CDC F - Envair - containment / for cancer drugs / for cytotoxics
Aseptic isolator - CDC F - Envair - containment / for cancer drugs / for cytotoxics - image - 2
Aseptic isolator - CDC F - Envair - containment / for cancer drugs / for cytotoxics - image - 3
Aseptic isolator - CDC F - Envair - containment / for cancer drugs / for cytotoxics - image - 4
Aseptic isolator - CDC F - Envair - containment / for cancer drugs / for cytotoxics - image - 5
Aseptic isolator - CDC F - Envair - containment / for cancer drugs / for cytotoxics - image - 6
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Characteristics

Applications
for cytotoxics, for cancer drugs, aseptic, containment, for hospitals
ISO class
ISO class 5
Type of products handled
for toxic products
Other characteristics
glove box, negative pressure, recirculating

Description

Overview
This negative-pressure isolator range is engineered to protect pharmacy and laboratory personnel from exposure to cytotoxic drugs while maintaining aseptic conditions for product protection. Units are suitable for sterile compounding, oncology pharmacy workflows and laboratory containment.

Applications
  • Preparation and compounding of cytotoxic and hazardous drugs
  • Oncology and hospital pharmacies
  • Research laboratories handling cytotoxic agents
  • Aseptic dispensing and small-batch sterile production


Configurations & options
  • Two-glove and four-glove configurations to match workflow and access requirements
  • Available working area widths: narrow and wide variants
  • Ducted or recirculating airhandling models; optional additional exhaust fans and filters
  • Transfer chambers with electromagnetic timed interlocks to minimise airborne contamination during transfers
  • PLC controls for configurable setup, operation and maintenance


Key features
  • Negative pressure containment for operator protection and safe handling of hazardous drugs
  • EU GMP Grade A unidirectional airflow work area (ISO 5 equivalent) for aseptic work and product protection
  • High air change rates and transfer chamber interlocks to suppress airborne contamination and speed evaporation of disinfectants
  • Automated pressure-decay leak test with indication and trend monitoring for containment verification
  • Design allowing safe replacement of the main (primary) filter and good access for cleaning


Caractéristiques / spécifications techniques
  • Model designation: CDC F
  • Containment: Negative-pressure isolator for cytotoxic handling
  • Work area classification: EU GMP Grade A unidirectional airflow (ISO 5 equivalent)
  • Glove options: 2-glove or 4-glove configurations
  • Airhandling options: Ducted or recirculating variants; additional exhaust fans and filters optional
  • Transfer: Transfer chambers with electromagnetic timed interlocks and high air change rates
  • Leak testing: Automated pressure-decay leak test with result indication and trend monitoring
  • Controls: PLC-based control system for setup, operation and maintenance
  • Maintenance: Safe replacement of main (primary) filter and good access for cleaning
  • Intended application: Safe handling of cytotoxic drugs and product protection from microbiological contamination
*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.
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