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Cerabalt K50

EUDAMED

Class IIa (EU MDR)

Ref 01105000Model CERABALT K50

by Bernard Cervos Societe

Identity

Trade Name
CERABALT K50 EUDAMED
Device Name
CERABALT K50 LINGOT EUDAMED
Model / Reference
CERABALT K50 EUDAMED
01105000 EUDAMED

Identifiers

Primary DI / UDI-DI
03760357970193 EUDAMED
Basic UDI-DI
376035797K50JG EUDAMED
EMDN Code
Q010601 DENTAL ALLOYS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

Yes

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

Cerabalt K50 by Bernard Cervos Societe — 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
FR-MF-000016213

Sources (1)

  • EUDAMED a93f9c20-bea5-4c6c-b725-af3a63f09c35 61 fields · synced Jul 17, 2026