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RegenKit-THT-T

EUDAMED

Class IIb (EU MDR)

Ref RK-THT-T

by Regen Lab SA

Identity

Trade Name
RegenKit-THT-T EUDAMED
Device Name
RegenKit-THT-T EUDAMED
Model / Reference
RK-THT-T EUDAMED

Identifiers

Primary DI / UDI-DI
07640138980893 EUDAMED
Basic UDI-DI
B-07640138980893 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

RegenKit-THT-T 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 4c6ffc35-44b1-48ed-86ad-07ceaf3e8f31 61 fields · synced Jul 13, 2026