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4500-126-000

by Stryker Corp.

Ref 4500-126-000Model 08858250000662S7

4500-126-000 is a Class I device made by Stryker Corp., registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 08858250000662S7) and listed in FDA GUDID since 28 May 2020 (UDI-DI 07613327467451), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858250000662S7 Basic UDI-DI 07613327467451UDI-DIDate4 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327467451 UDI-DI Date28 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000662S7 registered 4 Nov 2026 Active
  • FDA GUDID UDI-DI 07613327467451 listed 28 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327467451
  2. Registered EUDAMED 08858250000662S7

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  • Withdrawn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
Pin-driving power tool attachment
Device name
Universal Collets
Model / Ref / Catalog
4500-126-000, 08858250000662S7
Primary DI / UDI-DI
07613327467451
Basic UDI-DI
08858250000662S7
Direct marketing DI
07613327467451
FDA product code
HWE
EMDN code
Z12130580 Motorised orthopaedic surgery system instruments - hardware accessories
GMDN term
Pin-driving power tool attachment
Device class
Class I
Regulation number
878.4820
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Pin-driving power tool attachment

Similar devices in this category

Other devices filed under MOTORISED ORTHOPAEDIC SURGERY SYSTEM INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (21, all answered No)