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Lucea Led ®

FDA UDI

Class II (US FDA UDI)

by Maquet, Inc.

Identity

Trade Name
LUCEA LED ® FDA UDI
Generic Name
Operating room light FDA UDI
Device Name
POWER SUPPLY LCA 1 W FDA UDI
Model / Reference
ARD568604954 FDA UDI
Description
POWER SUPPLY LCA 1 W FDA UDI

Identifiers

Primary DI / UDI-DI
03700712405328 FDA UDI
FDA Product Code
NTN FDA UDI
FTD FDA UDI
GMDN Term
Operating room light FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
878.4580 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Operating room light

Lucea Led ® by Maquet, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maquet, Inc.

Sources (1)

  • FDA UDI ed936513-2c50-4484-9bc0-2fea52f4a928 33 fields · synced May 30, 2026