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Anchorage 705171

by Stryker GmbH

Ref 705171Model 08858251002524SR

Anchorage 705171 is a device classified as Class I in the EU and Class II in the US made by Stryker GmbH, registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 08858251002524SR) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 07613327131116), active as of 12 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251002524SR Basic UDI-DI 07613327131116UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327131116 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251002524SR registered 30 Oct 2026 Active
  • FDA GUDID UDI-DI 07613327131116 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327131116
  2. Registered EUDAMED 08858251002524SR

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  • Withdrawn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
Anchorage
Generic name
Orthopaedic trocar blade, reusable
Device name
Anchorage 2 Cp Instruments - Instrumentation Sleeves - Class I - Reusable - Non Sterile
Model / Ref / Catalog
705171, 08858251002524SR
Primary DI / UDI-DI
07613327131116
Basic UDI-DI
08858251002524SR
Direct marketing DI
07613327131116
FDA product code
HRS, HWC
EMDN code
P091280 Osteosynthesis devices, devices for tendon and ligament synthesis - accessories
GMDN term
Orthopaedic trocar blade, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
888.3030, 888.3040
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Orthopaedic trocar blade, reusable

Similar devices in this category

Other devices filed under OSTEOSYNTHESIS DEVICES, DEVICES FOR TENDON AND LIGAMENT SYNTHESIS - ACCESSORIES.

Other devices from Stryker GmbH

See all devices from Stryker GmbH →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Lot / batch number
Other properties (21, all answered No)