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M-Plast Gel compresses

EUDAMED

Class I (EU MDR)

Ref 297020Model 1422

by Ivf Hartmann Ag

Identity

Trade Name
M-Plast Gel compresses EUDAMED
Device Name
DermaPlast Compress Gel EUDAMED
Model / Reference
1422 EUDAMED
297020 EUDAMED

Identifiers

Primary DI / UDI-DI
07613312293461 EUDAMED
Basic UDI-DI
76116001422M4 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

M-Plast Gel compresses 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 26d25e5a-a567-43bd-aafa-8b3f611def88 61 fields · synced Oct 6, 2026