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DermaPlast Combifix

EUDAMED

Class I (EU MDR)

Ref 831150Model 1509

by Ivf Hartmann Ag

Identity

Trade Name
DermaPlast Combifix EUDAMED
Device Name
DermaPlast Combifix EUDAMED
Model / Reference
1509 EUDAMED
831150 EUDAMED

Identifiers

Primary DI / UDI-DI
07611600953516 EUDAMED
Basic UDI-DI
76116001509MH EUDAMED
EMDN Code
M040204 NON-ADHERENT ABSORBENT DRESSINGS EUDAMED

Classification

Device Class
Class I EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

DermaPlast Combifix by Ivf Hartmann Ag — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Ivf Hartmann Ag
EUDAMED SRN
CH-MF-000015962
Authorised Representative
PAUL HARTMANN AG DE-AR-000007519

Sources (1)

  • EUDAMED 0d89588b-f84f-4933-b313-8cca20328577 61 fields · synced Jun 18, 2026