Skip to content

LB83

by Steris Corporation

Ref LB83Model Sterile Light Handle Cover

LB83 is a device classified as Class I in the EU and Class II in the US made by Steris Corporation, registered in EUDAMED on 23 Sep 2026 (Basic UDI-DI 0724995MGSTERILLHCVRJ5) and listed in FDA GUDID since 14 May 2020 (UDI-DI 00724995172572), 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 Number0724995MGSTERILLHCVRJ5 Basic UDI-DI 00724995172572UDI-DIDate23 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995172572 UDI-DI Date14 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995MGSTERILLHCVRJ5 registered 23 Sep 2026 Active
  • FDA GUDID UDI-DI 00724995172572 listed 14 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00724995172572
  2. Registered EUDAMED 0724995MGSTERILLHCVRJ5

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  • Withdrawn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, single-use
Model / Ref / Catalog
LB83, Sterile Light Handle Cover
Primary DI / UDI-DI
00724995172572
Basic UDI-DI
0724995MGSTERILLHCVRJ5
FDA product code
FTA
EMDN code
Z12010785 Scialytic lamp lighting systems - consumables
GMDN term
Medical equipment handle cover, single-use
Device class
Class I EUDAMED
Class II GUDID
Regulation number
878.4580
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Medical equipment handle cover, single-use

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

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)