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0295726100

by Stryker Corp.

Ref 0295726100Model 08858250000328RQ

0295726100 is a Class I device made by Stryker Corp., registered in EUDAMED on 7 Oct 2026 (Basic UDI-DI 08858250000328RQ) and listed in FDA GUDID since 31 May 2020 (UDI-DI 07613327053050), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858250000328RQ Basic UDI-DI 07613327053050UDI-DIDate7 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327053050 UDI-DI Date31 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000328RQ registered 7 Oct 2026 Active
  • FDA GUDID UDI-DI 07613327053050 listed 31 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327053050
  2. Registered EUDAMED 08858250000328RQ

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  • Withdrawn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
Arthroscopic obturator
Device name
SMBU_TF10439_Drivers
Model / Ref / Catalog
0295726100, 08858250000328RQ
Primary DI / UDI-DI
07613327053050
Basic UDI-DI
08858250000328RQ
Direct marketing DI
07613327053050
FDA product code
FSM, NBH
EMDN code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
GMDN term
Arthroscopic obturator
Device class
Class I
Regulation number
878.4800, 888.1100
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Arthroscopic obturator

Similar devices in this category

Other devices filed under ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

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