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XTV006002

by Stryker GmbH

Ref XTV006002Model 08858251003008S9

XTV006002 is a surgical screwdriver (EU MDR Class IIa; FDA Class I; FDA product code HWE, Instrument, Surgical, Orthopedic, Ac-Powered Motor and Accessory/Attachment) made by Stryker GmbH, registered in EUDAMED on 9 Sep 2026 (Basic UDI-DI 08858251003008S9) and listed in FDA GUDID since 9 Jul 2020 (UDI-DI 07613252266938), active as of 12 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251003008S9 Basic UDI-DI 07613252266938UDI-DIDate9 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613252266938 UDI-DI Date9 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251003008S9 registered 9 Sep 2026 Active
  • FDA GUDID UDI-DI 07613252266938 listed 9 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613252266938
  2. Registered EUDAMED 08858251003008S9

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  • Withdrawn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
Fixos
Generic name
Surgical screwdriver, reusable
Device name
Fixos Instruments - Screwdrivers and Tightening Instrumentation - Class Iia - Non Sterile
Model / Ref / Catalog
XTV006002, 08858251003008S9
Primary DI / UDI-DI
07613252266938
Basic UDI-DI
08858251003008S9
Direct marketing DI
07613252266938
FDA product code
HWE
EMDN code
P091280 Osteosynthesis devices, devices for tendon and ligament synthesis - accessories
GMDN term
Surgical screwdriver, reusable
Device class
Class IIa EUDAMED
Class I GUDID
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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

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

Related devices

Category: Surgical screwdriver, reusable

Similar devices in this category

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

Other devices from Stryker GmbH

See all devices from Stryker GmbH →

Properties

  • Sterilise before use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)