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RACCORDO LLF doppio con alette

EUDAMED

Class I (EU MDR)

Ref SEP8102Model SEPLEX

by Meika Group S.r.l.

Identity

Device Name
RACCORDO LLF doppio con alette EUDAMED
Model / Reference
SEPLEX EUDAMED
SEP8102 EUDAMED

Identifiers

Primary DI / UDI-DI
08055348433432 EUDAMED
Basic UDI-DI
B-08055348433432 EUDAMED
EMDN Code
A070501 CAPS OR OBTURATORS, NON-PERFORABLE 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

RACCORDO LLF doppio con alette 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 6ea1549c-3097-496e-817f-68d90f9523af 61 fields · synced Jul 12, 2026