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6002-140-200

by Stryker Leibinger

Ref 6002-140-200Model 08858250000548S8

6002-140-200 is a Class I device made by Stryker Leibinger, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 08858250000548S8) and listed in FDA GUDID since 19 Feb 2025 (UDI-DI 07613327353563), 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 Number08858250000548S8 Basic UDI-DI 07613327353563UDI-DIDate27 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327353563 UDI-DI Date19 Feb 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000548S8 registered 27 Oct 2026 Active
  • FDA GUDID UDI-DI 07613327353563 listed 19 Feb 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327353563
  2. Registered EUDAMED 08858250000548S8

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  • Withdrawn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
Device sterilization/disinfection container, reusable
Model / Ref / Catalog
6002-140-200, 08858250000548S8
Primary DI / UDI-DI
07613327353563
Basic UDI-DI
08858250000548S8
Direct marketing DI
07613327353563
FDA product code
FSM
EMDN code
Z12011480 Surgical navigation instruments - hardware accessories
GMDN term
Device sterilization/disinfection container, reusable
Device class
Class I
Regulation number
878.4800
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: Device sterilization/disinfection container, reusable

Similar devices in this category

Other devices filed under SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES.

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Properties

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