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ARGEDENT 1 (20g)

EUDAMED

Class IIa (EU MDR)

Ref 130516

by The Argen Corporation

Identity

Device Name
ARGEDENT 1 (20g) EUDAMED
Model / Reference
130516 EUDAMED

Identifiers

Primary DI / UDI-DI
+D81813051601 EUDAMED
Basic UDI-DI
++D818DENTALALLOYS01GDP 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

Category: Dental casting non-noble alloy

ARGEDENT 1 (20g) by The Argen Corporation — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental casting non-noble alloy.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000022069
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED fb9e707c-e4b8-4d8e-90a3-b1b902df41bf 61 fields · synced Sep 17, 2026