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Medikro® Pro

EUDAMED

Class IIa (EU MDR)

Ref M915Model M9488

by Medikro Oy

Identity

Device Name
Medikro® Pro EUDAMED
Model / Reference
M9488 EUDAMED
M915 EUDAMED

Identifiers

Primary DI / UDI-DI
D-M9488SV EUDAMED
Basic UDI-DI
B-M9488SV EUDAMED
EMDN Code
Z12150101 CLINICAL/DIAGNOSTIC SPIROMETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Medikro® Pro by Medikro Oy — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Medikro Oy
EUDAMED SRN
FI-MF-000011841

Sources (1)

  • EUDAMED 12fdddc4-d8f3-4eaa-bbd6-54daacf37ecd 61 fields · synced May 23, 2026