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Cavigliera in neoprene con spirali laterali

EUDAMED

Class I (EU MDR)

Ref 642/JModel 642Ref 642, mis.L

by G.l.o. Srl

Identity

Device Name
Cavigliera in neoprene con spirali laterali EUDAMED
Model / Reference
642 EUDAMED
642/J EUDAMED
642, mis.L EUDAMED

Identifiers

Primary DI / UDI-DI
08051070436116 EUDAMED
08051070431135 EUDAMED
Basic UDI-DI
80510704364282 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

Cavigliera in neoprene con spirali laterali by G.l.o. Srl — 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
G.l.o. Srl
EUDAMED SRN
IT-MF-000018554

Sources (3)

  • EUDAMED 06ce1a42-7c9e-4f2f-aba5-0876c1c18974 61 fields · synced Jul 30, 2026
  • EUDAMED 0843e479-d27f-434a-991f-8451cf177d8d 61 fields · synced May 19, 2026
  • EUDAMED 0843e479-d27f-434a-991f-8451cf177d8d-1 61 fields · synced Jun 10, 2026