Xp Disposable Laryngoscope Blade Mac 2

by Heine Optotechnik GmbH & Co. KG

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	Number04053755129133 UDI-DI	Date11 Jan 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Xp Disposable Laryngoscope Blade Mac
Generic Name: Laryngoscope blade, single-use
Model / Ref / Catalog: 2, F-000.22.762

Primary DI / UDI-DI: 04053755129133
FDA Product Code: CCW
GMDN Term: Laryngoscope blade, single-use

Device Class: Class I
Regulation Number: 868.5540
GUDID distribution status: In Commercial Distribution

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Properties

Single Use
Premarket Exempt
Serial Number
Manufacturing Date

Other properties (10)

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
Expiration Date: No