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EZout 7202-200-049

by Stryker Corp.

Part of a family of 30 devices: see the family page

Ref 7202-200-049Model 08858250000673SC

EZout 7202-200-049 is a device classified as Class IIa in the EU and Class I in the US made by Stryker Corp., registered in EUDAMED on 15 Oct 2026 (Basic UDI-DI 08858250000673SC) and listed in FDA GUDID since 24 Sep 2017 (UDI-DI 07613327176025), 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 Number08858250000673SC Basic UDI-DI 07613327176025UDI-DIDate15 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327176025 UDI-DI Date24 Sep 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000673SC registered 15 Oct 2026 Active
  • FDA GUDID UDI-DI 07613327176025 listed 24 Sep 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327176025
  2. Registered EUDAMED 08858250000673SC

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  • Withdrawn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
EZout
Generic name
Sawing power tool attachment, sagittal
Model / Ref / Catalog
7202-200-049, 08858250000673SC
Primary DI / UDI-DI
07613327176025
Basic UDI-DI
08858250000673SC
Direct marketing DI
07613327176025
FDA product code
HWE
EMDN code
Z12130580 Motorised orthopaedic surgery system instruments - hardware accessories
GMDN term
Sawing power tool attachment, sagittal
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4820
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 IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Sawing power tool attachment, sagittal

Similar devices in this category

Other devices filed under MOTORISED ORTHOPAEDIC SURGERY SYSTEM INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)