Conquest Series 0300034601
Ref 0300-034-601Model 08858250000306RE
Conquest Series 0300034601 (0300-034-601) is a Class I device made by Stryker Corp., registered in EUDAMED on 6 Oct 2026 (Basic UDI-DI 08858250000306RE) and listed in FDA GUDID since 3 Aug 2018 (UDI-DI 07613327053425), active as of 25 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number08858250000306RE 07613327053425 | Date6 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07613327053425 | Date3 Aug 2018 | StatusListed |
Official records
- EUDAMED public site 08858250000306RE
- AccessGUDID record 07613327053425
Across registries
- EUDAMED Basic UDI-DI 08858250000306RE registered 6 Oct 2026 Active
- FDA GUDID UDI-DI 07613327053425 listed 3 Aug 2018 Listed
Timeline
- Listed FDA GUDID 07613327053425
- Registered EUDAMED 08858250000306RE
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Conquest Series
- Generic name
- Ligament reconstruction instrument set, reusable
- Device name
- SMBU_TF10436_Scissors
- Model / Ref / Catalog
- 08858250000306RE, 0300-034-601, 0300034601
- Primary DI / UDI-DI
- 07613327053425
- Basic UDI-DI
- 08858250000306RE
- Direct marketing DI
- 07613327053425
- 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
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 08858250000306RE 0300-034-601 | 0300034601 |
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