Ventilator filters and HMEs

DAR™ mechanical filter

<p>The DAR™ mechanical filter helps protect patients, equipment, and hospital staff from cross contamination.</p>

Features

  • End tidal carbon dioxide (CO2) sampling port offers convenient access for monitoring airway gases
  • Light weight, compact design reduces bulk in circuit
  • ISO standard 15 mm and 22 mm fitting connects with breathing circuit

Specifications

 

  Large–Sterivent Compact–Sterivent S Small–Sterivent mini
Tidal volume 300–1500 mL 200–1500 mL 150–1500 mL
Resistance to flow before use (ISO 9360-1) (ISO 23328-2)
15 L per minute 0.4 cmH2O 0.6 cmH2O
30 L per minute 0.8 cmH2O 0.9 cmH2O 1.2 cmH2O
60 L per minute 1.8 cmH2O 2.0 cmH2O 2.6 cmH2O
90 L per minute 3.0 cmH2O 3.2 cmH2O 4.2 cmH2O
Filtration efficiency
NaCl (ISO 23328-1) 99.973% 99.721% 99.478%
Bacterial Greater than or equal to 99.9999% Greater than or equal to
99.9999%
Greater than or equal to
99.9999%
Viral Greater than or equal to 99.9999% Greater than or equal to
99.9999%
Greater than or equal to
99.999%
Internal volume (ISO9360-1) (ISO 23328-1) 90 mL 68 mL 44 mL
Weight 49 g 39 g 25 g

Ordering information

DAR™ mechanical filters

Item number Size Patient end connection Machine end connection Units per box
351U5410 Large 22M/15F 22F/15M 50
351U5856 Large 22M 22F 50
351U5878 Compact 22M/15F 22F/15M 50
351U5979 Small 22M/15F 22F/15M 50

DAR™ mechanical filter accessories

Item number Description Filter end Machine end Units per box
332U5115 DAR™ extension tube 15F 15M 25
332U5663 DAR™ extendible extension tube 15F 15M 25
610U5257 DAR™ double-swivel connector 22M/15M 15M 50
331U5661 DAR™ double-swivel connector, extendible 22M/15M 15M 25

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All technical information is sourced from various information for use (IFU) documents and clinical evaluation reports. Please reference the instructions for use (IFU) for a complete product details.

† Internal testing Mirandola (various 2005– 2008). All technical information is sourced from information for use (IFU) documents PT00186626, PT00162624, and clinical evaluation report CER10055277. Please reference the IFU for complete product details.