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Prolunga Spiralata In Pvc No Dop

EUDAMED

Class I (EU MDR)

Ref S41530200.0Model PROLEX

by Meika Group S.r.l.

Identity

Device Name
PROLUNGA SPIRALATA IN PVC NO DOP EUDAMED
Model / Reference
PROLEX EUDAMED
S41530200.0 EUDAMED

Identifiers

Primary DI / UDI-DI
08055348432947 EUDAMED
Basic UDI-DI
B-08055348432947 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

Prolunga Spiralata In Pvc No Dop 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 83209dcf-f22f-4fe7-896a-0d23fb7d378e 61 fields · synced Jul 27, 2026