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Rampa 4 Vie 5 Fll + Llmg

EUDAMED

Class I (EU MDR)

Ref R40000000.3Model DEVIALEX

by Meika Group S.r.l.

Identity

Device Name
RAMPA 4 VIE 5 FLL + LLMG EUDAMED
Model / Reference
DEVIALEX EUDAMED
R40000000.3 EUDAMED

Identifiers

Primary DI / UDI-DI
08055348431193 EUDAMED
Basic UDI-DI
B-08055348431193 EUDAMED
EMDN Code
A0702 RAMPS 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

Rampa 4 Vie 5 Fll + Llmg 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 e026da64-5712-4850-bbff-9bc68c11fa1e 61 fields · synced Jul 30, 2026