H&H 30fr Nasopharyngeal Airway, Each 1.0

by H&H Medical Corporation

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00857048006552 UDI-DI	Date31 Dec 2020Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: H&H 30fr Nasopharyngeal Airway, Each
Generic Name: Nasopharyngeal airway, single-use
Model / Ref / Catalog: 1.0, HHNPA-EA

Primary DI / UDI-DI: 00857048006552
FDA Product Code: BTQ
GMDN Term: Nasopharyngeal airway, single-use

Device Class: Class I
Regulation Number: 868.5100
GUDID distribution status: In Commercial Distribution

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Properties

Single Use
Premarket Exempt

Other properties (12)

Sterile: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Lot / Batch Number: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No