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Kidz-750

EUDAMED

Class I (EU MDR)

Ref KIDZ-750V.XL

by F.G.P. s.r.l.

Identity

Trade Name
KIDZ-750 EUDAMED
Device Name
ORTESI PER CAVIGLIA-PIEDE PASSIVE - CAVIGLIA WALKER EUDAMED
Model / Reference
KIDZ-750V.XL EUDAMED

Identifiers

Primary DI / UDI-DI
08052990114528 EUDAMED
Basic UDI-DI
803348865Y0612060102VB EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES 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: Ankle/foot orthosis

Kidz-750 by F.G.P. s.r.l. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
F.G.P. s.r.l.
EUDAMED SRN
IT-MF-000043862

Sources (1)

  • EUDAMED a8d1197a-a9c1-44b8-8191-7fe432c38cde 61 fields · synced Jun 18, 2026