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G006/Mides

EUDAMED

Class I (EU MDR)

Ref G006/MIDESModel Ultrasound transmission gelRef G006

by FIAB S.p.A.

Identity

Model / Reference
Ultrasound transmission gel EUDAMED
G006/MIDES EUDAMED
G006 EUDAMED

Identifiers

Primary DI / UDI-DI
08058480759781 EUDAMED
08033003260234 EUDAMED
Basic UDI-DI
803300326130000012LE EUDAMED
803300326130000006LK 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

G006/Mides 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 (2)

  • EUDAMED 5bb49470-5afd-4883-98d8-e9e82263f647 61 fields · synced Jul 28, 2026
  • EUDAMED f3030b85-b4db-419c-be0f-0f257c82f30a 61 fields · synced May 17, 2026