AirLife RESNKBT01A

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10885403184536 UDI-DI	Date1 Sep 2016Listed	StatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: AirLife
Generic Name: Oxygen administration tubing
Model / Ref / Catalog: RESNKBT01A

Primary DI / UDI-DI: 10885403184536
FDA Product Code: OGG
GMDN Term: Oxygen administration tubing

Device Class: Class II
Regulation Number: 868.5450
GUDID distribution status: Not in Commercial Distribution

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Properties

Single Use
Prescription Use
Convenience Kit
Premarket Exempt
Lot / Batch Number

Other properties (9)

Sterile: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Combination Product: No
HCT/P: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No