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Fujifilm Lmp-001

by Fujifilm Corporation

Ref 04547410331127

Fujifilm Lmp-001 is a Class I device made by Fujifilm Corporation, registered in EUDAMED on 6 Oct 2026 (Basic UDI-DI 4547410201000000000005156) and listed in FDA GUDID since 7 Oct 2022 (UDI-DI 04547410331127), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4547410201000000000005156 Basic UDI-DI 04547410331127UDI-DIDate6 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04547410331127 UDI-DI Date7 Oct 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4547410201000000000005156 registered 6 Oct 2026 Active
  • FDA GUDID UDI-DI 04547410331127 listed 7 Oct 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04547410331127
  2. Registered EUDAMED 4547410201000000000005156

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Main Lamp LMP-001 EUDAMED
Fujifilm GUDID
Generic name
Procedural cold light bulb
Device name
Main Lamp 2
Model / reference
04547410331127 EUDAMED
LMP-001 GUDID
Description
This product is the lamp unit used in combination with our processor in medical facilities. Do not use this product for any other purpose.
Primary DI / UDI-DI
04547410331127
Basic UDI-DI
4547410201000000000005156
FDA product code
FFY
EMDN code
Z12029099 Various instruments for endoscopy and mini–invasive surgery – other
GMDN term
Procedural cold light bulb
Device class
Class I
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
04547410331127
GUDID
LMP-001

Related devices

Category: Procedural cold light bulb

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR ENDOSCOPY AND MINI–INVASIVE SURGERY – OTHER.

Other devices from Fujifilm Corporation

See all devices from Fujifilm Corporation →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)