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SET PER Preparazione o Somministrazione Farmaci

EUDAMED

Class I (EU MDR)

Ref MUL0074Model MULTIFLEX

by Meika Group S.r.l.

Identity

Device Name
SET PER Preparazione o Somministrazione Farmaci EUDAMED
Model / Reference
MULTIFLEX EUDAMED
MUL0074 EUDAMED

Identifiers

Primary DI / UDI-DI
08055348431575 EUDAMED
Basic UDI-DI
B-08055348431575 EUDAMED
EMDN Code
A03010199 INFUSION CONTROLLERS - OTHER 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

SET PER Preparazione o Somministrazione Farmaci 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 127c9f90-73cf-4e59-9960-e5ac538d0a67 61 fields · synced Jun 19, 2026