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29-20400

by Stryker Leibinger

Ref 29-20400Model 08858251001901SS

29-20400 is a Class I device made by Stryker Leibinger, registered in EUDAMED on 30 Jul 2026 (Basic UDI-DI 08858251001901SS) and listed in FDA GUDID since 8 Dec 2016 (UDI-DI 07613154170647), 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 Number08858251001901SS Basic UDI-DI 07613154170647UDI-DIDate30 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613154170647 UDI-DI Date8 Dec 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251001901SS registered 30 Jul 2026 Active
  • FDA GUDID UDI-DI 07613154170647 listed 8 Dec 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613154170647
  2. Registered EUDAMED 08858251001901SS

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  • Withdrawn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
Device name
Universal - MMF self drilling screw kit 2.0 + HMMF Storages
Model / Ref / Catalog
29-20400, 08858251001901SS
Primary DI / UDI-DI
07613154170647
Basic UDI-DI
08858251001901SS
Direct marketing DI
07613154170647
FDA product code
FSM
EMDN code
S010401 Trays, baskets, tubs for sterilisation and their components
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 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS.

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Properties

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