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AirLife™ 5708

by Vyaire Medical, Inc.

AirLife™ 5708 is a Class II device made by Vyaire Medical, Inc., listed in FDA GUDID since 4 Feb 2020 (UDI-DI 10190752147188), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10190752147188 UDI-DI Date4 Feb 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
AirLife™
Generic name
Heat/moisture exchanger, single-use
Model / Ref / Catalog
5708
Primary DI / UDI-DI
10190752147188
FDA product code
CAH
GMDN term
Heat/moisture exchanger, single-use
Device class
Class II
Regulation number
868.5260
GUDID distribution status
In Commercial Distribution

Related devices

Category: Heat/moisture exchanger, single-use

Similar devices in this category

Other devices filed under Heat/moisture exchanger, single-use.

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Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)