MK23 - Polycentric Pneumatic Knee Joint RIVO
by MOOR ORTOTIKA I PROTETIKA d.o.o. za izradu, doradu i trgovinu medicinskih i ortopedskih pomagala
Ref MK23Model MK23 - Polycentric Pneumatic Knee Joint "RIVO"
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 | Number3859894591MK23JR 03859894591906 | Date14 Sep 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- Withdrawn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
- Model / Reference
- MK23 - Polycentric Pneumatic Knee Joint "RIVO", MK23
- Primary DI / UDI-DI
- 03859894591906
- Basic UDI-DI
- 3859894591MK23JR
- Direct Marketing DI
- 03859894591906
- EMDN Code
- Y062415 Transfemoral prostheses (for amputation above knee)
- Device Class
- Class I
- EU market of registration
- Croatia
Manufacturer details
- EUDAMED SRN
- HR-MF-000056447
Other devices from MOOR ORTOTIKA I PROTETIKA d.o.o. za izradu, doradu i trgovinu medicinskih i ortopedskih pomagala
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