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Fujifilm

FDA UDI

Class I (US FDA UDI)

by FUJIFILM Corporation

Identity

Trade Name
FUJIFILM FDA UDI
Generic Name
Procedural cold light bulb FDA UDI
Device Name
This product is the lamp unit used in combination with our light source in medical facilities. Do not use this product for any other purpose. FDA UDI
Model / Reference
LMP-SD FDA UDI
Description
This product is the lamp unit used in combination with our light source in medical facilities. Do not use this product for any other purpose. FDA UDI

Identifiers

Primary DI / UDI-DI
04547410331752 FDA UDI
FDA Product Code
FFY FDA UDI
GMDN Term
Procedural cold light bulb FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Procedural cold light bulb

Fujifilm by FUJIFILM Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Procedural cold light bulb.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
FUJIFILM Corporation

Sources (1)

  • FDA UDI 39f46375-251c-49ee-8963-e674b9acbd87 35 fields · synced May 30, 2026