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Portaimpronte Perforati

EUDAMED

Class I (EU MDR)

Ref 60040Model PORTA IMPRONTE

by Gima Spa

Identity

Trade Name
PORTAIMPRONTE PERFORATI EUDAMED
Device Name
PORTA IMPRONTE EUDAMED
Model / Reference
PORTA IMPRONTE EUDAMED
60040 EUDAMED

Identifiers

Primary DI / UDI-DI
08023279600407 EUDAMED
Basic UDI-DI
80232790000V04020000000Q4 EUDAMED
EMDN Code
V0402 CLINICAL USE TRAYS AND BOWLS 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

Portaimpronte Perforati by Gima Spa — 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
Gima Spa
EUDAMED SRN
IT-MF-000011004

Sources (1)

  • EUDAMED e48eee45-0a8e-4fda-a8c2-c56469336d02 61 fields · synced Jul 31, 2026