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PROLUNGA PE Ø 1x2 Cm200 LLF/LLG SCHERMATA PER FARMACI FOTOSENSIBILI

EUDAMED

Class I (EU MDR)

Ref P51020200.2Model PROLEX

by Meika Group S.r.l.

Identity

Device Name
PROLUNGA PE Ø 1x2 Cm200 LLF/LLG SCHERMATA PER FARMACI FOTOSENSIBILI EUDAMED
Model / Reference
PROLEX EUDAMED
P51020200.2 EUDAMED

Identifiers

Primary DI / UDI-DI
08055348432817 EUDAMED
Basic UDI-DI
B-08055348432817 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 PE Ø 1x2 Cm200 LLF/LLG SCHERMATA PER FARMACI FOTOSENSIBILI 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 714b28d4-c697-4748-9e25-d4fb39c53fdd 61 fields · synced Oct 6, 2026