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LB23

by Steris Corporation

Ref LB23Model Sterilizable Light Handle

LB23 is a Class I device made by Steris Corporation, registered in EUDAMED on 10 Sep 2026 (Basic UDI-DI 0724995MGSTZBLGHTHANDY4) and listed in FDA GUDID since 2 Apr 2021 (UDI-DI 00724995152994), 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 Number0724995MGSTZBLGHTHANDY4 Basic UDI-DI 00724995152994UDI-DIDate10 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995152994 UDI-DI Date2 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995MGSTZBLGHTHANDY4 registered 10 Sep 2026 Active
  • FDA GUDID UDI-DI 00724995152994 listed 2 Apr 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00724995152994
  2. Registered EUDAMED 0724995MGSTZBLGHTHANDY4

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  • Withdrawn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

Generic name
Medical equipment handle cover, reusable
Device name
Sterilizable Light Handle
Model / Ref / Catalog
LB23, Sterilizable Light Handle
Primary DI / UDI-DI
00724995152994
Basic UDI-DI
0724995MGSTZBLGHTHANDY4
FDA product code
MDM
EMDN code
Z12010785 Scialytic lamp lighting systems - consumables
GMDN term
Medical equipment handle cover, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Medical equipment handle cover, reusable

Similar devices in this category

Other devices filed under SCIALYTIC LAMP LIGHTING SYSTEMS.

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Sterilise before use
  • Over-the-counter
  • Premarket exempt
  • Manufacturing date
Other properties (21, all answered No)