Skip to content

Fujifilm Lmp-Sd

by Fujifilm Corporation

Ref 04547410331752

Fujifilm Lmp-Sd is a Class I device made by Fujifilm Corporation, registered in EUDAMED on 6 Oct 2026 (Basic UDI-DI 454741020100000000000495K) and listed in FDA GUDID since 7 Oct 2022 (UDI-DI 04547410331752), 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 Number454741020100000000000495K Basic UDI-DI 04547410331752UDI-DIDate6 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04547410331752 UDI-DI Date7 Oct 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 454741020100000000000495K registered 6 Oct 2026 Active
  • FDA GUDID UDI-DI 04547410331752 listed 7 Oct 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04547410331752
  2. Registered EUDAMED 454741020100000000000495K

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  • Withdrawn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
SD Lamp LMP-SD EUDAMED
Fujifilm GUDID
Generic name
Procedural cold light bulb
Device name
SD Lamp 1
Model / reference
04547410331752 EUDAMED
LMP-SD GUDID
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.
Primary DI / UDI-DI
04547410331752
Basic UDI-DI
454741020100000000000495K
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
04547410331752
GUDID
LMP-SD

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)