Skip to content

62-50104

by Stryker Leibinger

Ref 62-50104Model 08858251028417UP

62-50104 is a Class I device made by Stryker Leibinger, registered in EUDAMED on 1 Oct 2026 (Basic UDI-DI 08858251028417UP) and listed in FDA GUDID since 24 Jan 2017 (UDI-DI 04546540538444), 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 Number08858251028417UP Basic UDI-DI 04546540538444UDI-DIDate1 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04546540538444 UDI-DI Date24 Jan 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251028417UP registered 1 Oct 2026 Active
  • FDA GUDID UDI-DI 04546540538444 listed 24 Jan 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04546540538444
  2. Registered EUDAMED 08858251028417UP

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  • Withdrawn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
Orthopaedic surgical procedure kit, non-medicated, reusable
Device name
VariSpeed Adapter
Model / Ref / Catalog
62-50104, 08858251028417UP
Primary DI / UDI-DI
04546540538444
Basic UDI-DI
08858251028417UP
Direct marketing DI
04546540538444
FDA product code
LXH
EMDN code
P091280 Osteosynthesis devices, devices for tendon and ligament synthesis - accessories
GMDN term
Orthopaedic surgical procedure kit, non-medicated, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic surgical procedure kit, non-medicated, reusable

Similar devices in this category

Other devices filed under OSTEOSYNTHESIS DEVICES, DEVICES FOR TENDON AND LIGAMENT SYNTHESIS - ACCESSORIES.

Other devices from Stryker Leibinger

  • 92-55772

    Class II

  • 92-55773

    Class II

  • 92-55771

    Class II

  • 92-55770

    Class II

See all devices from Stryker Leibinger →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)