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Dia-Ultrasonic

EUDAMED

Class I (EU MDR)

Ref POWER CORD / 4007-2075

by Diadent Group International

Identity

Trade Name
Dia-Ultrasonic EUDAMED
Device Name
Dia-Ultrasonic EUDAMED
Model / Reference
POWER CORD / 4007-2075 EUDAMED

Identifiers

Primary DI / UDI-DI
08806383586740 EUDAMED
Basic UDI-DI
88063835DUS5B EUDAMED
EMDN Code
Q0199 ODONTOLOGY DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Dia-Ultrasonic by Diadent Group International — 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
KR-MF-000023806
Authorised Representative
Diadent Europe B.V. NL-AR-000012597

Sources (1)

  • EUDAMED a32dccbf-3e36-4aad-8ead-e8983d386585 61 fields · synced Jul 16, 2026