← Back to catalogue

RegenACR-C Plus

EUDAMED

Class IIb (EU MDR)

Ref R-ACR C/BA

by Regen Lab SA

Identity

Trade Name
RegenACR-C Plus EUDAMED
Device Name
RegenACR-C Plus EUDAMED
Model / Reference
R-ACR C/BA EUDAMED

Identifiers

Primary DI / UDI-DI
07640138980336 EUDAMED
Basic UDI-DI
B-07640138980336 EUDAMED
EMDN Code
B0501,B0599 EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

RegenACR-C Plus by Regen Lab Sa — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Regen Lab SA
EUDAMED SRN
CH-MF-000032231
Authorised Representative
RegenLab France FR-AR-000011953

Sources (1)

  • EUDAMED ae1c4d1c-e34f-4187-ba78-0d113a9f75f1 61 fields · synced Jun 19, 2026