M Air T Air Testing Systems

Description

   • M Air T portable air tester
   • M Air T air testers for isolators and compressed gas
   • Ready-to-use cassettes, prefilled with medium, gamma-sterilized, double-sleeve packaged, certificate included
   • Easy-to-use, compact, lightweight sampler, programmable, extended-life battery, delay timer to minimize risk of secondary contamination
   • USP and EP compliance certificate
   • Simple colony counting through integrated grid
   • Fast and reliable results with maximum recovery; large agar amount and unique micro-perforated sieve allow air sampling of up to 1 cubic meter
   • Reproducible results; unit-to-unit consistency of agar surface shape

A lightweight air tester featuring a unique cassette design for determining the presence of viable, airborne microorganisms in critical areas. The system impacts microorganisms onto an agar surface, which is the referenced method for analyzing microbial air contamination (USP 28-NF 23, 1st Supplement, EU-GMP guidelines).

Calibration made easy

Air monitoring systems must be calibrated in order to conform to Good Manufacturing Practices. You can let our service specialists calibrate your M Air T system, or you can do it yourself using the M Air T calibration kit. The kit contains everything you need: flow meter, flow rate correction table, instruction manual, calibration sieve, and calibration certificate.

Air Monitoring in Isolators

The M Air T isolator system brings the convenience and performance of the M Air T concept to isolators and barrier environments. This portable system consists of a programmable pump, which remains outside the controlled area, and an independent sampling head, which uses prefilled M Air T agar cassettes.

Specifications (return to top)

Validation support

Comprehensive protocols are available to make validation faster and easier. The validation protocol book contains ready-to-use installation and operation qualification protocols that are written to the same standards as the protocols used to validate pharmaceutical processes.