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DermaPlast Compress Gel

EUDAMED

Class I (EU MDR)

Ref 218720Model 1422

by Ivf Hartmann Ag

Identity

Trade Name
DermaPlast Compress Gel EUDAMED
Device Name
DermaPlast Compress Gel EUDAMED
Model / Reference
1422 EUDAMED
218720 EUDAMED

Identifiers

Primary DI / UDI-DI
07611600953585 EUDAMED
Basic UDI-DI
76116001422M4 EUDAMED
Unit of Use DI
07611600996292 EUDAMED
EMDN Code
M040204 NON-ADHERENT ABSORBENT DRESSINGS 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 Compress Gel 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 7cb749a4-aa9a-45a7-9bd0-7be8c8df6e60 61 fields · synced Oct 6, 2026