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Gomitiera

EUDAMED

Class I (EU MDR)

Ref 613, mis.SModel 613

by G.l.o. Srl

Identity

Device Name
Gomitiera EUDAMED
Model / Reference
613 EUDAMED
613, mis.S EUDAMED

Identifiers

Primary DI / UDI-DI
08051566282647 EUDAMED
Basic UDI-DI
805156628613D4 EUDAMED
EMDN Code
Y060615 ELBOW 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

Gomitiera 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 08020e3d-1f0f-43d7-a401-b11733c59e4c 61 fields · synced Jul 8, 2026
  • EUDAMED 08020e3d-1f0f-43d7-a401-b11733c59e4c-1 61 fields · synced Jun 10, 2026