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5407-476-000

by Stryker Corp.

Ref 5407-476-000Model 08858250000677SL

5407-476-000 is a Class I device made by Stryker Corp., registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI 08858250000677SL) and listed in FDA GUDID since 20 Oct 2020 (UDI-DI 07613327510768), 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 Number08858250000677SL Basic UDI-DI 07613327510768UDI-DIDate2 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327510768 UDI-DI Date20 Oct 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000677SL registered 2 Nov 2026 Active
  • FDA GUDID UDI-DI 07613327510768 listed 20 Oct 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327510768
  2. Registered EUDAMED 08858250000677SL

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  • Withdrawn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
Signature Sterilization Trays
Model / Ref / Catalog
5407-476-000, 08858250000677SL
Primary DI / UDI-DI
07613327510768
Basic UDI-DI
08858250000677SL
Direct marketing DI
07613327510768
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
Netherlands
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.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

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