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P41025200.0

EUDAMED

Class I (EU MDR)

Ref P41025200.0Model PROLEX

by Meika Group S.r.l.

Identity

Device Name
P41025200.0 EUDAMED
Model / Reference
PROLEX EUDAMED
P41025200.0 EUDAMED

Identifiers

Primary DI / UDI-DI
08055348432497 EUDAMED
Basic UDI-DI
B-08055348432497 EUDAMED
EMDN Code
A03020101 LOW PRESSURE EXTENSION LINES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

P41025200.0 by Meika Group S.r.l. — Class I — 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
Meika Group S.r.l.
EUDAMED SRN
IT-MF-000029106

Sources (1)

  • EUDAMED d3291a3c-d240-46e3-9ef1-04b728ae0b8f 61 fields · synced Jun 18, 2026