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ArthroVisc40 Kit

EUDAMED

Class 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 EUDAMED
ARV-HA40-1 EUDAMED

Identifiers

Primary DI / UDI-DI
07640138980350 EUDAMED
07640138981470 EUDAMED
Basic UDI-DI
B-07640138980350 EUDAMED
B-07640138981470 EUDAMED
EMDN Code
P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Czechia EUDAMED
Germany 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

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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