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Riskontrol Kavo E

EUDAMED

Class I (EU MDR)

Ref 200172

by Acteon Manufacturing

Identity

Trade Name
RISKONTROL KAVO E EUDAMED
Device Name
RISKONTROL adapter EUDAMED
Model / Reference
200172 EUDAMED

Identifiers

Primary DI / UDI-DI
03760243000201 EUDAMED
Basic UDI-DI
376024300adaptateurTU EUDAMED
EMDN Code
Q0199 ODONTOLOGY DEVICES - OTHER EUDAMED

Classification

Device Class
Class I 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

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

Riskontrol Kavo E by Acteon Manufacturing — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
FR-MF-000007556

Sources (1)

  • EUDAMED 4dcb6f4f-a48c-4fc1-b878-594ea5830c68 61 fields · synced Jul 13, 2026