← Back to catalogue

Phyloetek Stabimed® Pro

EUDAMED

Class I (EU MDR)

Ref PY-TKST PROV.M

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

Identity

Trade Name
PHYLOETEK STABIMED® PRO EUDAMED
Device Name
ORTESI PER GINOCCHIO - GINOCCHIERE EUDAMED
Model / Reference
PY-TKST PROV.M EUDAMED

Identifiers

Primary DI / UDI-DI
08052990115242 EUDAMED
Basic UDI-DI
803348865Y06120902CT EUDAMED
EMDN Code
Y061209 KNEE 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

Phyloetek Stabimed® Pro 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

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

Manufacturer

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

Sources (1)

  • EUDAMED df015473-c85c-4b84-ae51-332886c301c7 61 fields · synced Jun 18, 2026