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Rampa A 3 Vie 4 Fll+ Llm

EUDAMED

Class I (EU MDR)

Ref R30000000.2Model DEVIALEX

by Meika Group S.r.l.

Identity

Device Name
RAMPA A 3 VIE 4 FLL+ LLM EUDAMED
Model / Reference
DEVIALEX EUDAMED
R30000000.2 EUDAMED

Identifiers

Primary DI / UDI-DI
08055348431117 EUDAMED
Basic UDI-DI
B-08055348431117 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 A 3 Vie 4 Fll+ Llm 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 e8daa294-d245-4e1a-a5eb-6c90a42fd870 61 fields · synced Jun 19, 2026