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Hoffmann 4933-1-022

by Stryker Corp.

Ref 4933-1-022Model 08858251002853TF

Hoffmann 4933-1-022 is a device classified as Class I in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 14 Jul 2026 (Basic UDI-DI 08858251002853TF) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07613252610335), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251002853TF Basic UDI-DI 07613252610335UDI-DIDate14 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613252610335 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251002853TF registered 14 Jul 2026 Active
  • FDA GUDID UDI-DI 07613252610335 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613252610335
  2. Registered EUDAMED 08858251002853TF

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  • Withdrawn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
Hoffmann LRF™ EUDAMED
Hoffmann GUDID
Generic name
External orthopaedic fixation system noninvasive component, single-use
Device name
Hlrf - Adapters and Bolts - Class I - Non Sterile
Model / Ref / Catalog
4933-1-022, 08858251002853TF
Primary DI / UDI-DI
07613252610335
Basic UDI-DI
08858251002853TF
FDA product code
KTT
EMDN code
P09120499 External bone fixation systems - other
GMDN term
External orthopaedic fixation system noninvasive component, single-use
Device class
Class I EUDAMED
Class II GUDID
Regulation number
888.3030
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Related devices

Category: External orthopaedic fixation system, reusable

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (21, all answered No)