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Mekasense tuntotesteri

EUDAMED

Class I (EU MDR)

Ref PL-13010

by Mekalasi Oy

Identity

Trade Name
Mekasense tuntotesteri EUDAMED
Device Name
Mekasense tuntotesteri EUDAMED
Model / Reference
PL-13010 EUDAMED

Identifiers

Primary DI / UDI-DI
06430074263577 EUDAMED
Basic UDI-DI
6430074265465VY EUDAMED
EMDN Code
V0399 MEASUREMENT DEVICES - OTHER 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

Mekasense tuntotesteri 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 48d6098f-f360-44ad-946d-d825b33185b3 61 fields · synced Jul 9, 2026