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DermaPlast Compress Plus

EUDAMED

Class I (EU MDR)

Ref 550311Model 3295Ref 550301

by Ivf Hartmann Ag

Identity

Trade Name
DermaPlast Compress Plus EUDAMED
Device Name
DermaPlast Compress Plus EUDAMED
Model / Reference
3295 EUDAMED
550311 EUDAMED
550301 EUDAMED

Identifiers

Primary DI / UDI-DI
07611600953455 EUDAMED
07611600953448 EUDAMED
Basic UDI-DI
76116003295N3 EUDAMED
Unit of Use DI
07611600996322 EUDAMED
07611600996315 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 Plus 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 (2)

  • EUDAMED 33529634-9007-4b50-b322-f0bf45ec5257 61 fields · synced Jul 9, 2026
  • EUDAMED e94cd76a-3b27-4eb4-90fe-ac293221cdef 61 fields · synced May 18, 2026