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Kohottaja

EUDAMED

Class I (EU MDR)

Ref PL-13501

by Mekalasi Oy

Identity

Trade Name
Kohottaja EUDAMED
Device Name
Kohottaja EUDAMED
Model / Reference
PL-13501 EUDAMED

Identifiers

Primary DI / UDI-DI
06430074262877 EUDAMED
Basic UDI-DI
6430074265328VM EUDAMED
EMDN Code
U089010 UTERINE CURETTES, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

Kohottaja by Mekalasi Oy — 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

Manufacturer
Mekalasi Oy
EUDAMED SRN
FI-MF-000003102

Sources (1)

  • EUDAMED 78496fcf-2534-4914-8875-704e8a920ac0 61 fields · synced Jun 17, 2026