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9102550140

by Stryker Corp.

Ref 9102-550-140Model 08858251028112TW

9102550140 (9102-550-140) is a device classified as Class IIa in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI 08858251028112TW) and listed in FDA GUDID since 16 Jun 2025 (UDI-DI 37613327592994), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251028112TW Basic UDI-DI 37613327592994UDI-DIDate20 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number37613327592994 UDI-DI Date16 Jun 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251028112TW registered 20 Oct 2026 Active
  • FDA GUDID UDI-DI 37613327592994 listed 16 Jun 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 37613327592994
  2. Registered EUDAMED 08858251028112TW

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  • Withdrawn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
Sterilization container filter, single-use
Device name
Sterile Battery Container Filter Packs
Model / Ref / Catalog
08858251028112TW, 9102-550-140, 9102550140
Primary DI / UDI-DI
37613327592994
Basic UDI-DI
08858251028112TW
Unit of use DI
07613327592993
FDA product code
KCT
EMDN code
S9099 Sterilisation devices (excluding cat. d - z) - other
GMDN term
Sterilization container filter, single-use
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
08858251028112TW
9102-550-140
GUDID
9102550140
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: Sterilization container filter, single-use

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

  • Single use
  • Over-the-counter
  • Lot / batch number
Other properties (22, all answered No)