 |
|
|
|
Product Category : Environmental Monitoring
CanistAIR™ D/A
|
Drying and Adsorption System for Microbial Sampling of Hazardous Drug Environments The non-invasive CanistAIR D/A System was developed to ensure the maintenance of proper aseptic and hazardous containment techniques during compounding, while assuring the safe recovery of hazardous vapors and fumes generated during in-process sampling. The sampling pump air stream may be vented to the room without contamination of the pump, or reintroduction of the contaminated pump exhaust back into an active PEC sterile compounding zone. This system facilitates proper asepsis, and the isolation and containment of hazardous drug residues aspirated during sampling. The CanistAIR D/A consists of separate desiccant and adsorption canisters to be assembled sequentially, external to the PEC, in-line with the EnviroAssay BioCassette Microbial Sampling System. Includes standard transport and assembly procedures for quick and effective in-process sampling, and proper disposal. ..........................................................
CAD $72.50
Package of Two Cartridges
(Not Sold Separately)
|
|
|
|
Non-invasive sampling of the in-process hazardous drug environment in the manner designated by USP <797> and pharmaceutical industry standards requires complete extraction of the microbial sample volume from the Primary Engineering Control (PEC) BSC or CACI critical compounding area through the sampling pump. In accord with USP <797>, no self-powered sampler should ever be used in these critical areas, due to both the considerable disturbance of the airflow patterns introduced by a non-sterile sampler within the critical work zone, and the accrual of sampler surface and internal contamination with hazardous substances. Also, no contaminated pump exhaust air stream containing hazardous drug residues, particulates, aerosols of oil, and condensates should ever be re-introduced back into a BSC at any point or location during in-process sterile compounding activities--even peripherally: This practice constitutes a blatant violation of proper aseptic and containment techniques, and has not been validated as a proper or effective disposal method. Recovery of the potentially-contaminated microbial sample must, therefore, be quiescently accomplished from the critical work zone and vented safely outside the PEC.
|
BioCassette T-Tryptic Soy
Agar with Development
EnviroAssay DPC Kit
Lighthouse 3016 Handheld
Particle Counter
|
|
|
|  |
 |
|
 |
