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1068-056-000

by Stryker Corp.

Ref 1068-056-000Model 08858250000299SA

1068-056-000 is a device classified as Class I in the EU and Class II in the US made by Stryker Corp., registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI 08858250000299SA) and listed in FDA GUDID since 10 Sep 2020 (UDI-DI 07613327504347), 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 Number08858250000299SA Basic UDI-DI 07613327504347UDI-DIDate16 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327504347 UDI-DI Date10 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000299SA registered 16 Jun 2026 Active
  • FDA GUDID UDI-DI 07613327504347 listed 10 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327504347
  2. Registered EUDAMED 08858250000299SA

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  • Withdrawn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
Arm procedure positioner, reusable
Device name
Accessories: Arm Board
Model / Ref / Catalog
1068-056-000, 08858250000299SA
Primary DI / UDI-DI
07613327504347
Basic UDI-DI
08858250000299SA
Direct marketing DI
07613327504347
FDA product code
FPO
EMDN code
V08068099 Medical beds - other accessories
GMDN term
Arm procedure positioner, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6910
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

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: Arm procedure positioner, reusable

Similar devices in this category

Other devices filed under MEDICAL BEDS - OTHER ACCESSORIES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Premarket exempt
  • Serial number
Other properties (23, all answered No)