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AirLife™ 603RAH

by Airlife, Inc.

AirLife™ 603RAH is a Class I device made by Airlife, Inc., listed in FDA GUDID since 22 Aug 2022 (UDI-DI 10190752154940), 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 Number10190752154940 UDI-DI Date22 Aug 2022ListedStatusListed 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  • Withdrawn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
Arterial blood sampling kit
Model / Ref / Catalog
603RAH
Primary DI / UDI-DI
10190752154940
FDA product code
OFP
GMDN term
Arterial blood sampling kit
Device class
Class I
Regulation number
868.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Arterial blood sampling kit

Other devices from Airlife, Inc.

See all devices from Airlife, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)