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Ginocchiera in neoprene

EUDAMED

Class I (EU MDR)

Ref 610/F, mis.MModel 610

by G.l.o. Srl

Identity

Device Name
Ginocchiera in neoprene EUDAMED
Model / Reference
610 EUDAMED
610/F, mis.M EUDAMED

Identifiers

Primary DI / UDI-DI
08051070430077 EUDAMED
Basic UDI-DI
8051070436107M 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

Ginocchiera in neoprene by G.l.o. Srl — 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
G.l.o. Srl
EUDAMED SRN
IT-MF-000018554

Sources (2)

  • EUDAMED 93a4ed74-9939-4701-824e-b13c1683f3bc 61 fields · synced Jun 18, 2026
  • EUDAMED 93a4ed74-9939-4701-824e-b13c1683f3bc-1 61 fields · synced Jun 10, 2026