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KENTAMED ACTIS-150a

EUDAMED

Class IIb (EU MDR)

Ref 10-11-02

by KENTAMED Ltd.

Identity

Trade Name
KENTAMED ACTIS-150a EUDAMED
Device Name
KENTAMED ACTIS-150 EUDAMED
Model / Reference
10-11-02 EUDAMED

Identifiers

Primary DI / UDI-DI
03800943000191 EUDAMED
Basic UDI-DI
3800943ACTIS150P4 EUDAMED
Direct Marketing DI
03800943000191 EUDAMED
EMDN Code
Z12010902 ELECTROSURGICAL UNITS (ESU) FOR GENERAL USE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Bulgaria 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

Category: Foot-switch, electrical

KENTAMED ACTIS-150a by KENTAMED Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Foot-switch, electrical.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
KENTAMED Ltd.
EUDAMED SRN
BG-MF-000022619

Sources (1)

  • EUDAMED dbfc55e0-ca7c-4c3d-a44a-3b5c32a8541a 61 fields · synced Aug 3, 2026