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Air Sampler optimized to GMP

SAS SUPER ISO 100/180

Product features

  • Satisfies USP Chapter 1116 and ISO 14698-1
  • Provides IQ, OQ validation protocol
  • Collects up to 70,000 L of air and stores 300 sampling cycles
  • Accurate sampling rate maintained by speed sensor installation
  • Structure to prevent turbulence and measured air re-inhalation of one-way air flow
  • Easy and simply key pad
  • Automatic notification when instrument calibration expires
  • Can be collected while charging the battery
  • Provides traceability

WHY USE THE SAS SUPER ISO

  • 180L of air can be collected per minute, reducing sampling time by 45% compared to 100L
  • Lightweight, durable,
    and easy portability
  • Convenient and intuitive
    touch keypad

Product specification

SAS SUPER ISO 100 SAS SUPER ISO 180
Flux 100LPM 180LPM
1000L collection time 10min 5.5min
Battery capacity 70,000L (for 1 time charge) 40,000L (for 1 time charge)
Battery time Approx. 11 hours Approx. 4 hours
Speed sensor O
Interval sampling Possible
Delay sampling Possible
Weight 1.8Kg
Size 120×125×275 mm (W x L x H)
Compatible head Aluminum, stainless steel, sterile plastic (disposable)
Compatible medium Petri dish (90mm) / Contact plate (55mm)
Data output Can be downloaded on PC in various formats (USB C-type))
Product warranty 2 years

액세사리

  • Single-use heads
    for air samplers
  • Adapter for
    Petri dishes Ø 90 mm
  • Battery charger with
    interchangeable plug
  • Infrared
    remote control
  • Stainless steel floor tripod Extendable from 1000 up to 20000 mm high
  • Stainless steel holder
    for table and wall

Compliance with regulation

  1. 1. USP chapter 1116 ‘Microbiological evaluation of clean rooms and controlled environment’
  2. 2. EU guide for GMP – ‘Manufacture of sterile medicinal products control medicines and inspection’
  3. 3. ISO Standard 14698-1 ‘Cleanrooms and associated controlled environments biocontamination control – Part 1: General principles and methods’
  4. 4. FDA – ‘2004 guidance for industry on sterile drug products by aseptic processing – Pharmaceutical current good manufacturing practice’