Skip to Content Skip to Main menu

Air Sampler

Home
Inquiry

Can reduce work time by up to 70%

DUO SAS SUPER 360

Product features

  • Satisfies USP Chapter 1116 and ISO 14698-1
  • Provides IQ, OQ validation protocol
  • Collects up to 40,000 L of air and stores 100 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 DUAL HEAD?

  • Up to 70% reduction in sampling time by collecting 360L of air per minute through dual heads
    (1000L - 2 minutes 45 seconds /
    2000L – 5 minutes 30 seconds)
  • When using TSA medium on the left and
    SDA medium on the right,
    bacterial/fungal monitoring
    can be done simultaneously
  • A more reliable colony forming unit (CFU)
    can be derived by calculating the average value when using the same medium
    on the left and right sides

Product specification

SAS SUPER DUO 360
Flux 360LPM (180LPM+180LPM)
2000L collection time 5.5min
Battery capacity 40,000L (for 1 time charge)
Battery time Approx. 2 hours
Speed sensor O
Interval sampling Possible
Delay sampling Possible
Weight 2.2Kg
Size 260×110×352 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

Accessories

  • 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. ACGIH – ‘Guideline for assessment of bioaerosol in the indoor environment’
  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’