Autogenous Osteochondral Grafting System, 8mm
by Double Medical Technology Inc.
Ref 117436000S
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number6902139QX01003KU 06942836194260 | Date3 Nov 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Autogenous Osteochondral Grafting System,8mm
- Model / reference
- 117436000S
- Primary DI / UDI-DI
- 06942836194260
- Basic UDI-DI
- 6902139QX01003KU
- EMDN code
- K030212 Arthroscopy instrument kits, single use
- Device class
- Class IIa
- EU registration type
- Standard device
- EU market of registration
- Hungary
Manufacturer details
- EUDAMED SRN
- CN-MF-000009048
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Double Medical Technology Inc.
Properties
Other properties (13)
- Sterilise before use: No
- Implantable: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No