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Prolunga 2 Vie Per Infusione Simultanee

EUDAMED

Class I (EU MDR)

Ref MUL0039Model MULTIFLEX

by Meika Group S.r.l.

Identity

Device Name
PROLUNGA 2 VIE PER INFUSIONE SIMULTANEE EUDAMED
Model / Reference
MULTIFLEX EUDAMED
MUL0039 EUDAMED

Identifiers

Primary DI / UDI-DI
08055348431520 EUDAMED
Basic UDI-DI
B-08055348431520 EUDAMED
EMDN Code
A03020199 EXTENSIONS - 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

Prolunga 2 Vie Per Infusione Simultanee 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 dd3f3166-ab38-4cb6-aae6-16ff22473601 61 fields · synced Jul 14, 2026