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9102763030

by Stryker Corp.

Ref 9102-763-030Model 08858251006163TB

9102763030 (9102-763-030) is a device classified as Class IIa in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 21 Oct 2026 (Basic UDI-DI 08858251006163TB) and listed in FDA GUDID since 12 Jun 2025 (UDI-DI 07613327487541), 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 Number08858251006163TB Basic UDI-DI 07613327487541UDI-DIDate21 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327487541 UDI-DI Date12 Jun 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251006163TB registered 21 Oct 2026 Active
  • FDA GUDID UDI-DI 07613327487541 listed 12 Jun 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327487541
  2. Registered EUDAMED 08858251006163TB

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  • Withdrawn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
System 9
Generic name
Device sterilization/disinfection container, reusable
Device name
Sterile Battery Container Lids and Bases
Model / Ref / Catalog
08858251006163TB, 9102-763-030, 9102763030
Primary DI / UDI-DI
07613327487541
Basic UDI-DI
08858251006163TB
Direct marketing DI
07613327487541
FDA product code
KCT
EMDN code
S9099 Sterilisation devices (excluding cat. d - z) - other
GMDN term
Device sterilization/disinfection container, reusable
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
880.6850
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
08858251006163TB
9102-763-030
GUDID
9102763030
Device classEUDAMED
Class IIa
GUDID
Class II

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

Related devices

Category: Device sterilization/disinfection container, reusable

Similar devices in this category

Other devices filed under STERILISATION DEVICES (EXCLUDING CAT. D - Z) - OTHER.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Over-the-counter
  • Lot / batch number
Other properties (23, all answered No)