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Molla di Codivilla modificata cuoio

EUDAMED

Class I (EU MDR)

Ref 30/3 dx, mis.38Model 30

by G.l.o. Srl

Identity

Device Name
Molla di Codivilla modificata cuoio EUDAMED
Model / Reference
30 EUDAMED
30/3 dx, mis.38 EUDAMED

Identifiers

Primary DI / UDI-DI
08055965379847 EUDAMED
Basic UDI-DI
80559653730UH 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

Yes

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Ankle/foot orthosis

Molla di Codivilla modificata cuoio 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 (2)

  • EUDAMED c8369b6c-fa59-469a-8ef5-4eaf93dfb080 61 fields · synced Jun 20, 2026
  • EUDAMED c8369b6c-fa59-469a-8ef5-4eaf93dfb080-1 61 fields · synced Jun 10, 2026