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RegenACR-C Extra

EUDAMED

Class IIb (EU MDR)

Ref R-ACR C2/B

by Regen Lab SA

Identity

Trade Name
RegenACR-C Extra EUDAMED
Device Name
RegenACR-C Extra EUDAMED
Model / Reference
R-ACR C2/B EUDAMED

Identifiers

Primary DI / UDI-DI
07640138980176 EUDAMED
Basic UDI-DI
B-07640138980176 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 Extra 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

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Manufacturer

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

Sources (1)

  • EUDAMED beb702a3-58a4-49f9-b53e-53f0985f6661 61 fields · synced Jul 17, 2026