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G016/Amistim

EUDAMED

Class I (EU MDR)

Ref G016/AMISTIMModel RF cream

by FIAB S.p.A.

Identity

Model / Reference
RF cream EUDAMED
G016/AMISTIM EUDAMED

Identifiers

Primary DI / UDI-DI
08058480753611 EUDAMED
Basic UDI-DI
803300326130000011LC EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

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

Category: Device sterilization/disinfection container, reusable

G016/Amistim by FIAB S.p.A. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

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 1ce28985-589f-417e-a929-e4dce0764ffe 61 fields · synced Jul 13, 2026