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ArthroVisc40 Kit
EUDAMEDClass III (EU MDR)
Ref ARV-HA40-3Ref ARV-HA40-1
by Regen Lab SA
Identity
- Trade Name
- ArthroVisc40 Kit EUDAMED
- Device Name
- ArthroVisc40 Kit EUDAMED
- Model / Reference
- ARV-HA40-3 EUDAMEDARV-HA40-1 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07640138980350 EUDAMED07640138981470 EUDAMED
- Basic UDI-DI
- B-07640138980350 EUDAMEDB-07640138981470 EUDAMED
- EMDN Code
- P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Czechia EUDAMEDGermany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
EUDAMED
Reusable
No
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
ArthroVisc40 Kit by Regen Lab Sa — Class III — 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-07640138980350 | Class III | Active |
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Manufacturer
- Manufacturer
- Regen Lab SA
- EUDAMED SRN
- CH-MF-000032231
- Authorised Representative
- RegenLab France FR-AR-000011953
Sources (2)
- EUDAMED 533514b9-bdc7-4ad3-81b6-bd149889fe1f 61 fields · synced Jul 31, 2026
- EUDAMED 94675bbf-0abc-450d-a47f-06803c11491b 61 fields · synced May 18, 2026