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Miconvey

EUDAMED

Class IIb (EU MDR)

Ref K500

by Miconvey Technologies Co., Ltd.

Identity

Trade Name
Miconvey EUDAMED
Device Name
Ultrasonic Surgical Generator EUDAMED
Model / Reference
K500 EUDAMED

Identifiers

Primary DI / UDI-DI
06974710250915 EUDAMED
Basic UDI-DI
697471025K500E8 EUDAMED
EMDN Code
Z12010801 ULTRASONIC SCALPEL EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy 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

Miconvey by Miconvey Technologies Co., Ltd. — Class IIb — 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
CN-MF-000031532
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED bd2b8d7a-566a-48b2-b19f-7dfd60a2ef0e 61 fields · synced Jun 9, 2026