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0206564000

by Stryker Corp.

Ref 0206-564-000Model 08858251002447SY

0206564000 (0206-564-000) is a Class I device made by Stryker Corp., registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI 08858251002447SY) and listed in FDA GUDID since 24 Sep 2018 (UDI-DI 04546540858283), active as of 7 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251002447SY Basic UDI-DI 04546540858283UDI-DIDate26 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04546540858283 UDI-DI Date24 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251002447SY registered 26 Oct 2026 Active
  • FDA GUDID UDI-DI 04546540858283 listed 24 Sep 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04546540858283
  2. Registered EUDAMED 08858251002447SY

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  • Withdrawn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
Orthopaedic cement curette
Model / Ref / Catalog
08858251002447SY, 0206-564-000, 0206564000
Primary DI / UDI-DI
04546540858283
Basic UDI-DI
08858251002447SY
FDA product code
JDZ
EMDN code
P099002 Orthopaedic cement preparation and application devices and kits
GMDN term
Orthopaedic cement curette
Device class
Class I
Regulation number
888.4210
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
Model / referenceEUDAMED
08858251002447SY
0206-564-000
GUDID
0206564000

Related devices

Category: Orthopaedic cement curette

Similar devices in this category

Other devices filed under ORTHOPAEDIC CEMENT PREPARATION AND APPLICATION DEVICES AND KITS.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)