Ortimplant
by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi 1,000+ variants
Ref O100 02 228 0014
Active
CE MDD
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/MDD | NumberB-08680941143688 08680941143688 | Date16 Feb 2024 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device name
- 4,5 Mm Kavi̇sli̇ Rekonstrüksi̇yon Plak Çeli̇k 14 Deli̇k (4,5 Mm Curved Reconstruction Plate Ss 14 Holes)
- Model / reference
- O100 02 228 0014
- Primary DI / UDI-DI
- 08680941143688
- Basic UDI-DI
- B-08680941143688
- EMDN code
- P09120501 Osteosynthesis compression plates
- Device class
- Class IIb
- System or procedure pack
- System which is a device in itself
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000017438
Other devices from Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi
See all devices from Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi →
Properties
Other properties (10)
- Supplied sterile: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No