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Asnis 45-30006S

by Stryker Corp.

Ref 45-30006SModel 08858251002975TW

Asnis 45-30006S is a device classified as Class IIa in the EU and Class I in the US made by Stryker Corp., registered in EUDAMED on 17 Aug 2026 (Basic UDI-DI 08858251002975TW) and listed in FDA GUDID since 22 Sep 2016 (UDI-DI 04546540534224), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251002975TW Basic UDI-DI 04546540534224UDI-DIDate17 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04546540534224 UDI-DI Date22 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251002975TW registered 17 Aug 2026 Active
  • FDA GUDID UDI-DI 04546540534224 listed 22 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04546540534224
  2. Registered EUDAMED 08858251002975TW

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  • Withdrawn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
Asnis
Generic name
Bone tap, single-use
Device name
Asnis Micro Instruments - Tapping Instrumentation - Class Iia - Sterile
Model / Ref / Catalog
45-30006S, 08858251002975TW
Primary DI / UDI-DI
04546540534224
Basic UDI-DI
08858251002975TW
Direct marketing DI
07613327375480
FDA product code
HTW
EMDN code
P091280 Osteosynthesis devices, devices for tendon and ligament synthesis - accessories
GMDN term
Bone tap, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Length — 80.0 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Related devices

Category: Bone tap, single-use

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)