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Antidecubito ginocchio

EUDAMED

Class I (EU MDR)

Ref 700/A

by G.l.o. Srl

Identity

Device Name
Antidecubito ginocchio EUDAMED
Model / Reference
700/A EUDAMED

Identifiers

Primary DI / UDI-DI
08051070439704 EUDAMED
Basic UDI-DI
805107043700AUC 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 ginocchio 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 899b378c-a8eb-4893-8967-f4b51bd95162 61 fields · synced Jul 25, 2026