Orti̇mplant
by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi 1,000+ variants
Ref O600 10 153 0019Model O911 11 100 0000
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8683206OFIX000018N 08683206659603 | Date9 Feb 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Femur -Tibia T-Klemp (Femur -Tibia T-Clamp)
- Model / Reference
- O911 11 100 0000, O600 10 153 0019
- Primary DI / UDI-DI
- 08683206659603
- Basic UDI-DI
- 8683206OFIX000018N
- Direct Marketing DI
- 08683206659603
- EMDN Code
- P09120499 External bone fixation systems - other
- Device Class
- Class I
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- TR-MF-000017438
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Properties
Other properties (13)
- Sterile: No
- Implantable: No
- 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