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DIAfresh

EUDAMED

Class I (EU MDR)

Ref 26-0031Model 485

by PRISMAN GmbH

Identity

Trade Name
DIAfresh EUDAMED
Device Name
Prothesen Finish PLUS EUDAMED
Model / Reference
485 EUDAMED
26-0031 EUDAMED

Identifiers

Primary DI / UDI-DI
04064797028018 EUDAMED
Basic UDI-DI
++EPRM485EN EUDAMED
EMDN Code
P0199 PROSTHESES, FACIAL, ODONTOLOGICAL, AND CRANIAL - OTHERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

DIAfresh by PRISMAN GmbH — 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
PRISMAN GmbH
EUDAMED SRN
DE-MF-000009900

Sources (1)

  • EUDAMED 28f716ab-69fd-421e-a697-10871fcbcec9 61 fields · synced Jul 30, 2026