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CERABALT K30 Neutre

EUDAMED

Class IIa (EU MDR)

Ref 1103009Model CERABALT K30

by Bernard Cervos Societe

Identity

Trade Name
CERABALT K30 Neutre EUDAMED
Device Name
LINGOT CERABALT K30 EUDAMED
Model / Reference
CERABALT K30 EUDAMED
1103009 EUDAMED

Identifiers

Primary DI / UDI-DI
03760357974030 EUDAMED
Basic UDI-DI
376035797K30JA 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 K30 Neutre 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 81191a63-3841-4d80-9319-eec31b787709 61 fields · synced Jun 18, 2026