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DermaPlast Alginat

EUDAMED

Class I (EU MDR)

Ref 601510Model 3206

by Ivf Hartmann Ag

Identity

Trade Name
DermaPlast Alginat EUDAMED
Device Name
Alginate EUDAMED
Model / Reference
3206 EUDAMED
601510 EUDAMED

Identifiers

Primary DI / UDI-DI
07611600601516 EUDAMED
Basic UDI-DI
76116003206MA EUDAMED
EMDN Code
M04040201 ALGINATE DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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 Alginat 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 ed63aa73-c305-4752-b7d1-8c48c0a306aa 61 fields · synced Jun 19, 2026