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Conquest Series 0300034101

by Stryker Corp.

Part of a family of 35 devices: see the family page

Ref 0300-034-101Model 08858250000304RA

Conquest Series 0300034101 (0300-034-101) is a Class I device made by Stryker Corp., registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI 08858250000304RA) and listed in FDA GUDID since 3 Aug 2018 (UDI-DI 07613327053210), 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 Number08858250000304RA Basic UDI-DI 07613327053210UDI-DIDate5 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613327053210 UDI-DI Date3 Aug 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858250000304RA registered 5 Oct 2026 Active
  • FDA GUDID UDI-DI 07613327053210 listed 3 Aug 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613327053210
  2. Registered EUDAMED 08858250000304RA

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  • Withdrawn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
Conquest Series
Generic name
Ligament reconstruction instrument set, reusable
Device name
SMBU_TF10436_Punches
Model / Ref / Catalog
08858250000304RA, 0300-034-101, 0300034101
Primary DI / UDI-DI
07613327053210
Basic UDI-DI
08858250000304RA
Direct marketing DI
07613327053210
FDA product code
NBH
EMDN code
L090999 Orthopaedic surgery cutting instruments, reusable - other
GMDN term
Ligament reconstruction instrument set, reusable
Device class
Class I
Regulation number
888.1100
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Outer Diameter — 3.4 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
08858250000304RA
0300-034-101
GUDID
0300034101

Related devices

Category: Ligament reconstruction instrument set, reusable

Similar devices in this category

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

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (19, all answered No)