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Remotion 910-1003

by Stryker GmbH

Ref 910-1003Model 08858251002619T5

Remotion 910-1003 is a Class I device made by Stryker GmbH, registered in EUDAMED on 18 Aug 2026 (Basic UDI-DI 08858251002619T5) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 00886385010496), 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 Number08858251002619T5 Basic UDI-DI 00886385010496UDI-DIDate18 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00886385010496 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251002619T5 registered 18 Aug 2026 Active
  • FDA GUDID UDI-DI 00886385010496 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00886385010496
  2. Registered EUDAMED 08858251002619T5

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  • Withdrawn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
Re-Motion EUDAMED
Remotion GUDID
Generic name
General internal orthopaedic fixation system implantation kit
Device name
Re-Motion Instruments - Implant Shaping Instrumentation - Class I - Reusable - Non Sterile
Model / Ref / Catalog
910-1003, 08858251002619T5
Primary DI / UDI-DI
00886385010496
Basic UDI-DI
08858251002619T5
Direct marketing DI
00886385010496
FDA product code
HXZ
EMDN code
P090380 Wrist prostheses - accessories
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: General internal orthopaedic fixation system implantation kit

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES, OSTEOSYNTHESIS DEVICES, DEVICES FOR TENDON AND LIGAMENT SYNTHESIS.

Other devices from Stryker GmbH

See all devices from Stryker GmbH →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)