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Airlife AF5040MBM5

by Ventlab Corp.

Airlife AF5040MBM5 is a Class II device made by Ventlab Corp., listed in FDA GUDID since 15 Oct 2026 (UDI-DI 10889483654286), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10889483654286 UDI-DI Date15 Oct 2026ListedStatusListed 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  • Withdrawn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
Pulmonary resuscitator, manual, single-use
Model / reference
AF5040MBM5
Primary DI / UDI-DI
10889483654286
FDA product code
BTM
GMDN term
Pulmonary resuscitator, manual, single-use
Device class
Class II
Regulation number
868.5915
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Other devices from Ventlab Corp.

See all devices from Ventlab Corp. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)