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Antidecubito gomito

EUDAMED

Class I (EU MDR)

Ref 700/G

by G.l.o. Srl

Identity

Device Name
Antidecubito gomito EUDAMED
Model / Reference
700/G EUDAMED

Identifiers

Primary DI / UDI-DI
08051070439711 EUDAMED
Basic UDI-DI
805107043700GUQ EUDAMED
EMDN Code
V0811 HEEL, ELBOW AND KNEE ANTI-DECUBITUS PROTECTION AIDS 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

Antidecubito gomito 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 (1)

  • EUDAMED 43764d20-f25c-4fec-a637-ee3f31480bbd 61 fields · synced Jul 31, 2026