Genus
by Adler Ortho S.p.A 1,000+ variants
Ref 1759000Model GENUS PS FIXED TIBIAL PLUG
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-08052536561175 08052536561175 | Date10 Sep 2026 | 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- Withdrawn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
- Austria
- Belgium
- Bulgaria
- Croatia
- Cyprus
- Czechia
- Denmark
- Estonia
- Finland
- France
- Germany
- Greece
- Hungary
- Iceland
- Ireland
- Italy
- Latvia
- Liechtenstein
- Lithuania
- Luxembourg
- Malta
- Netherlands
- Northern Ireland
- Norway
- Poland
- Portugal
- Romania
- Slovakia
- Slovenia
- Spain
- Sweden
- Türkiye
Specification
- Model / reference
- GENUS PS FIXED TIBIAL PLUG, 1759000
- Primary DI / UDI-DI
- 08052536561175
- Basic UDI-DI
- B-08052536561175
- EMDN code
- P09098003 Knee prostheses obturators and plugs
- Device class
- Class III
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000010164
Other devices from Adler Ortho S.p.A
Properties
Other properties (10)
- Sterilise before use: 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