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Apribocca Pedo In Silicone Arancio

EUDAMED

Class I (EU MDR)

Ref 825/AModel DISPOSITIVI MEDICI PER USO ODONTOIATRICO

by MEDESY srl

Identity

Trade Name
APRIBOCCA PEDO IN SILICONE ARANCIO EUDAMED
Model / Reference
DISPOSITIVI MEDICI PER USO ODONTOIATRICO EUDAMED
825/A EUDAMED

Identifiers

Primary DI / UDI-DI
08054036140959 EUDAMED
Basic UDI-DI
805660060MEDFT01IL9 EUDAMED
Direct Marketing DI
08054036140959 EUDAMED
EMDN Code
L150299 ODONTOSTOMATOLOGY SPREADERS AND RETRACTORS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Apribocca Pedo In Silicone Arancio by MEDESY 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
MEDESY srl
EUDAMED SRN
IT-MF-000028737

Sources (1)

  • EUDAMED fe12522c-334d-4fa9-9a04-01ddd9b4d19a 61 fields · synced Jul 25, 2026