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F7830/Adtek30

EUDAMED

Class I (EU MDR)

Ref F7830/ADTEK30Model Adapter cables

by FIAB S.p.A.

Identity

Model / Reference
Adapter cables EUDAMED
F7830/ADTEK30 EUDAMED

Identifiers

Primary DI / UDI-DI
08058480758012 EUDAMED
Basic UDI-DI
803300326105000028MR EUDAMED
EMDN Code
Z12050680 NON-IMPLANTABLE CARDIAC STIMULATORS - HARDWARE ACCESSORIES 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

F7830/Adtek30 by FIAB S.p.A. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
FIAB S.p.A.
EUDAMED SRN
IT-MF-000005988

Sources (1)

  • EUDAMED 069ea534-30bb-41f0-a1eb-cb2d4c4de8e8 61 fields · synced Aug 3, 2026