← Back to catalogue

Helioform H Konzentrat

EUDAMED

Class IIa (EU MDR)

Ref 7351

by C.HAFNER GmbH + Co. KG

Identity

Trade Name
Helioform H Konzentrat EUDAMED
Device Name
Galvanoprodukte EUDAMED
Model / Reference
7351 EUDAMED

Identifiers

Primary DI / UDI-DI
04251936500867 EUDAMED
Basic UDI-DI
425193650000000002X5 EUDAMED
Direct Marketing DI
04251936500867 EUDAMED
EMDN Code
Q010601 DENTAL ALLOYS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

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

Helioform H Konzentrat by C.HAFNER GmbH + Co. KG — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000006304

Sources (1)

  • EUDAMED c82a6f6b-b6f7-45c5-a441-3bed5e3460ea 61 fields · synced Jul 9, 2026