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Rubinetto A 1 Via

EUDAMED

Class I (EU MDR)

Ref R10000000.1Model DEVIALEX

by Meika Group S.r.l.

Identity

Device Name
RUBINETTO A 1 VIA EUDAMED
Model / Reference
DEVIALEX EUDAMED
R10000000.1 EUDAMED

Identifiers

Primary DI / UDI-DI
08055348430875 EUDAMED
Basic UDI-DI
B-08055348430875 EUDAMED
EMDN Code
A0703 STOPCOCKS 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

Rubinetto A 1 Via 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 f50972e7-5caf-4551-8a41-630af7184302 61 fields · synced Jun 19, 2026