AxSOS
Ref 370001SModel 08858251006742TZ
Withdrawn
CE MDR, withdrawn
Ended
Withdrawn
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number08858251006742TZ 07613154089437 | Date2 Sep 2026 | StatusWithdrawn |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Withdrawn
Specification
- Device Name
- Axsos - Insert - Stainless Steel - Class Iib - Sterile
- Model / Reference
- 08858251006742TZ, 370001S
- Primary DI / UDI-DI
- 07613154089437
- Basic UDI-DI
- 08858251006742TZ
- EMDN Code
- P09120699 Bone fixation screws, tendon and ligament synthesis screws - other
- Device Class
- Class IIb
Manufacturer details
- EUDAMED SRN
- CH-MF-000009332
- Authorised representative
- Stryker European Operations Limited IE-AR-000000092
Other devices from Stryker GmbH
Properties
Other properties (11)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No