ARD569203932

by Maquet, Inc.

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	Number03700712413569 UDI-DI	Date29 Mar 2022Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Operating room light
Model / reference: ARD569203932

Primary DI / UDI-DI: 03700712413569
FDA product code: FTA
GMDN term: Operating room light

Device class: Class II
Regulation number: 878.4580
GUDID distribution status: In Commercial Distribution

MRI safety: MR Unsafe

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Properties

Premarket exempt
Serial number
Manufacturing date

Other properties (12)

Supplied sterile: No
Sterilise before use: No
Single use: 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