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Abformpfosten

EUDAMED

Class I (EU MDR)

Ref MGAR2301HModel Abformpfosten

by OrangeCAD Med GmbH

Identity

Device Name
Abformpfosten EUDAMED
Model / Reference
Abformpfosten EUDAMED
MGAR2301H EUDAMED

Identifiers

Primary DI / UDI-DI
04262365196163 EUDAMED
Basic UDI-DI
42623651912615181321147B4 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 OrangeCAD MED 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
OrangeCAD Med GmbH
EUDAMED SRN
DE-MF-000023347

Sources (1)

  • EUDAMED e3ae681a-dbd9-4577-bf77-bd3fb9247e7a 61 fields · synced Jun 19, 2026