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Covision
EUDAMEDClass I (EU MDR)
Ref 95.1602CModel REFLECTO REVISION KNEE SYSTEM INSTRUMENTS CASE 3
Identity
- Trade Name
- COVISION EUDAMED
- Device Name
- REFLECTO REVISION KNEE SYSTEM INSTRUMENTS CASE 3 EUDAMED
- Model / Reference
- REFLECTO REVISION KNEE SYSTEM INSTRUMENTS CASE 3 EUDAMED95.1602C EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05051659204689 EUDAMED
- Basic UDI-DI
- B-05051659204689 EUDAMED
- EMDN Code
- L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Covision by Covision Medical Technologies Ltd. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05051659204689 | Class I | Active |
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Manufacturer
- Manufacturer
- Covision Medical Technologies Ltd.
- EUDAMED SRN
- GB-MF-000025081
- Authorised Representative
- Covision Medical Technologies (Ireland) Limited IE-AR-000031129
Sources (1)
- EUDAMED 6f616e0c-b71c-4f3d-82a6-1d624591cc2e 61 fields · synced Jun 19, 2026