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Gnl-800 Rr

EUDAMED

Class I (EU MDR)

Ref EGNL-800 RRV.S

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

Identity

Trade Name
GNL-800 RR EUDAMED
Device Name
ORTESI PER GINOCCHIO - GINOCCHIERE EUDAMED
Model / Reference
EGNL-800 RRV.S EUDAMED

Identifiers

Primary DI / UDI-DI
08033609578207 EUDAMED
Basic UDI-DI
803348865Y06120902CT EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal 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

Gnl-800 Rr by F.G.P. s.r.l. — 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
F.G.P. s.r.l.
EUDAMED SRN
IT-MF-000043862

Sources (1)

  • EUDAMED a2f0bea0-fbb5-4d7e-a639-574d040001a4 61 fields · synced Jul 17, 2026