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Kit Introduzione

EUDAMED

Class IIa (EU MDR)

Ref EAK10

by Alfamed Srl

Identity

Device Name
KIT INTRODUZIONE EUDAMED
Model / Reference
EAK10 EUDAMED

Identifiers

Primary DI / UDI-DI
08056479540167 EUDAMED
Basic UDI-DI
B-08056479540167 EUDAMED
EMDN Code
N02010101 EPIDUROSCOPY AND EPIDUROPLASTICS CATHETERS AND KITS EUDAMED

Classification

Device Class
Class IIa 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Kit Introduzione by Alfamed Srl — Class IIa — 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
Alfamed Srl
EUDAMED SRN
IT-MF-000033580

Sources (1)

  • EUDAMED aa0c7794-86ac-4a48-8f53-50a7884c280b 61 fields · synced Jul 13, 2026