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Abformpfosten

EUDAMED

Class I (EU MDR)

Ref 23.168.33.000Model Abformpfosten

by Heliocos GmbH

Identity

Device Name
Abformpfosten EUDAMED
Model / Reference
Abformpfosten EUDAMED
23.168.33.000 EUDAMED

Identifiers

Primary DI / UDI-DI
04251923106256 EUDAMED
Basic UDI-DI
4251923112615181321147LU EUDAMED
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY 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

Abformpfosten by Heliocos 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
Heliocos GmbH
EUDAMED SRN
DE-MF-000006272

Sources (1)

  • EUDAMED 9d67ae1b-a609-4c8e-917c-3cc61d8e78a0 61 fields · synced Oct 6, 2026