6007-104-150
Ref 6007-104-150Model 08858250000550RT
6007-104-150 is a device classified as Class IIa in the EU and Class II in the US made by Stryker Leibinger, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI 08858250000550RT) and listed in FDA GUDID since 21 Sep 2016 (UDI-DI 34546540503238), active as of 7 Nov 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 | Number08858250000550RT 34546540503238 | Date6 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number34546540503238 | Date21 Sep 2016 | StatusListed |
Official records
- EUDAMED public site 08858250000550RT
- AccessGUDID record 34546540503238
Across registries
- EUDAMED Basic UDI-DI 08858250000550RT registered 6 Nov 2026 Active
- FDA GUDID UDI-DI 34546540503238 listed 21 Sep 2016 Listed
Timeline
- Listed FDA GUDID 34546540503238
- Registered EUDAMED 08858250000550RT
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- OrthoLock
- Generic name
- Orthopaedic bone pin, non-bioabsorbable
- Device name
- OrthoLock EX-Pins
- Model / Ref / Catalog
- 6007-104-150, 08858250000550RT
- Primary DI / UDI-DI
- 34546540503238
- Basic UDI-DI
- 08858250000550RT
- Unit of use DI
- 04546540503237
- FDA product code
- HAW, OLO
- EMDN code
- Z12011485 Surgical navigation instruments - consumables
- GMDN term
- Orthopaedic bone pin, non-bioabsorbable
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 882.4560
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 150.0 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class II |
| Implantable | No | Yes |
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