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MatriDerm

EUDAMED

Class III (EU MDR)

Ref 83403-200Model MatriDerm

by Medskin Solutions Dr. Suwelack AG

Identity

Trade Name
MatriDerm EUDAMED
Device Name
MatriDerm Dermal Matrix EUDAMED
Model / Reference
MatriDerm EUDAMED
83403-200 EUDAMED

Identifiers

Primary DI / UDI-DI
04250569300035 EUDAMED
Basic UDI-DI
B-04250569300035 EUDAMED
EMDN Code
P900404 AUTOLOGOUS GRAFT SUPPORTS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
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

Yes

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

MatriDerm by MedSkin Solutions Dr. Suwelack AG — 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

EUDAMED SRN
DE-MF-000007747

Sources (1)

  • EUDAMED f8f24548-65fe-44da-996b-64ff0679e3fd 61 fields · synced May 23, 2026