1. All Products
  2. HIGH-FLOW HEATED RESPIRATORY HUMIDIFIER (AIRVO 2)
Public Pricelist

HIGH-FLOW HEATED RESPIRATORY HUMIDIFIER (AIRVO 2)

https://unicat.msf.org/cat/product/80501
NST EEMDHRHE2--

Valid Article

CE marking: declaration that the product meets EU standards for health, safety, and environmental protection. The CE marking indicates that the product may be sold freely in any part of the European Economic Area, regardless of its country of origin.
R060202 - Oxygen administration humidification systems
European Medical Device Nomenclature (EMDN) is the nomenclature of use by manufacturers when registering their medical devices in the EUDAMED database. EMDN is characterised by its alphanumeric structure that is established in a seven-level hierarchical tree.
IIa
In Europe, medical material that fulfills the definition of a medical device according to the MDR (Medical Device Regulation) is classified into 4 classes
P
The order of this product needs to be justified and is only acceptable under certain conditions.
OC subscriptions: included in supply or field order tools (e.g. UniField)
SC subscriptions: included in supply or field tools
OC validations: approved for procurement and use by an OC for international or local orders specifying context and activity in Medical Standard Lists (MSL)

This combination does not exist.

See Related

Add article to list

   
Create Cancel

Add Kit To Wishlist

   
Create Cancel

HIGH-FLOW HEATED RESPIRATORY HUMIDIFIER (AIRVO 2)

Definition

A mains electricity (AC-powered) device designed for the treatment of spontaneously breathing patients who would benefit from receiving high-flow (typically greater than 15 L/min) heated and humidified ambient air or an air/oxygen mixtures. The gases are delivered to the patient's airway via the nose/mouth or a tracheostoma.

It typically consists of a gas flow generator, a heating element, humidification chamber, and breathing tube(s).

Specifications

Some restricted information has been hidden. Sign in to see this information

Components

  • Tube and chamber kit
    • Auto-fill water chamber MR290
    • Heated breathing tube
  • Interface adaptors
    • tracheostomy direct connection OPT870
    • mask interface adaptor 22 mm RT013
  • Hospital stand 900PT42
  • Pole mounting tray 900PT405
  • Oxygen inlet extension kit 900PT422
  • ​Filter holder 900PT912
  • Air filter 900PT913
Image

Technical specifications

  • ​Supply Frequency: 50/60 Hz
  • Supply Voltage: 230 V~ 1.8 A
  • Supply Current: 1.0 A max at 230 V~1.8 A
  • Heater Plate: 150 W
  • Heater Wire:22 V~, 2.73 A, 60 W , 50/60 Hz
  • Heater Plate Over-temperature Cutout: 118 ± 6 °C
  • Sound pressure level: Alarms exceed 45dbA @ 1 m
  • ​Auditory alarm pause 115 seconds
  • Humidification performances
    • >33 mg/l at 27°C target
    • >12mg/l at 34°C target
    • >12mg/l at 31°C target
  • Maximum temperature of delivered gas : 43°C (109°F)
  • Maximum flow range: 10-60 l/min (default); 2-25 l/min (Junior mode)
  • Maximum oxygen input: 60l/min
  • Warm-up time:
    • 10 minutes to 31 °C (88 °F),
    • 30 minutes to 37 °C (98.6 °F)
    • using a MR290 chamber with flow rate of 35 L/min and starting temperature 23 ± 2 °C (73 ± 3 °F)
  • Oxygen analyzer accuracy: < ± 4% of gas level) within the range 25-95% O2
  • Operating conditions:
    • 18-28 °C (64-82 °F),
    • 10-95% RH
    • Altitude 0 to 2000 m (6000 feet)
  • Protection against electric shock
    • Type B
    • Class II double insulated

Dimensions

  • 295 mm x 170 mm x 175 mm (11.6 in x 6.7 in x 6.9 in)
  • Weight:
    • 2.2 kg (4.8 lb) unit only,
    • 3.4 kg (7.5 lb) packaged in bag incl. accessories

To be Ordered Separately

Patient interface:

  • nasal cannula: infant, paediatric, adult S/M/L
  • oxygen mask
  • tracheostomy tube

Instructions for use

The input of this flowmeter is French standard NF and the wall outlet will need to compatible, otherwise an adapter will be required. Contact your OC Biomed for clarification

MSF requirements

For the treatment of spontaneously breathing patients who would benefit from receiving high flow warmed and humidified respiratory gases, in the Coronavirus epidemics.

Some restricted information has been hidden. Sign in to see this information
Some restricted information has been hidden. Sign in to see this information

Description approved by referents of OCP (Ribhar Ndouba) and OCB (Jonathan Delchambre) in August 2022.