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Abformpfosten

EUDAMED

Class I (EU MDR)

Ref 23.274.30.011Model Abformpfosten

by Heliocos GmbH

Identity

Device Name
Abformpfosten EUDAMED
Model / Reference
Abformpfosten EUDAMED
23.274.30.011 EUDAMED

Identifiers

Primary DI / UDI-DI
04251923107543 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

Category: Dental implant suprastructure, temporary, preformed, single-use

Abformpfosten by Heliocos GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

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 389ed033-5c72-4a3d-b6e6-4043605dde47 61 fields · synced Jun 19, 2026