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7900126000

by Stryker Corp.

Ref 7900-126-000Model 08858250000611RN

7900126000 (7900-126-000) is a Class I device made by Stryker Corp., registered in EUDAMED on 26 Jun 2026 (Basic UDI-DI 08858250000611RN) and listed in FDA GUDID since 19 Dec 2025 (UDI-DI 07613327643824), 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 Number08858250000611RN Basic UDI-DI 07613327643824UDI-DIDate26 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327643824 UDI-DI Date19 Dec 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000611RN registered 26 Jun 2026 Active
  • FDA GUDID UDI-DI 07613327643824 listed 19 Dec 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327643824
  2. Registered EUDAMED 08858250000611RN

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  • Withdrawn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
Collets
Model / Ref / Catalog
08858250000611RN, 7900-126-000, 7900126000
Primary DI / UDI-DI
07613327643824
Basic UDI-DI
08858250000611RN
Direct marketing DI
07613327643824
FDA product code
HWE
EMDN code
Z12019080 Various instruments for general and multidisciplinary surgery - 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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
08858250000611RN
7900-126-000
GUDID
7900126000

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - HARDWARE ACCESSORIES.

Other devices from Stryker Corp.

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Properties

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