← Back to catalogue

G999

EUDAMED

Class I (EU MDR)

Ref G999Model Medical conductive and abrasive paste

by FIAB S.p.A.

Identity

Model / Reference
Medical conductive and abrasive paste EUDAMED
G999 EUDAMED

Identifiers

Primary DI / UDI-DI
08058480757763 EUDAMED
Basic UDI-DI
803300326130000015LL 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

G999 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 75057c76-e544-473a-9cfc-ced90c7127e1 61 fields · synced Jul 21, 2026