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Data last updated: Apr 2025

URIKI BOARD

B-03770027558026

On MarketUnknown

RegulationEU MDR

ManufacturerIki

Primary DI03770027558026

ReferenceURIKI BOARD

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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Identification

Primary DI03770027558026

Basic UDI-DIB-03770027558026

ReferenceURIKI BOARD

Issuing Agency—

ULIDM2NMNGEZ

Classification

Risk ClassUnknown

RegulationEU MDR

StatusOn Market

Device TypesComing soon

Manufacturer

ManufacturerIki

Manufacturer SRNFR-MF-000023181

Manufacturer StatusActive

CND Nomenclature

V0599CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER

Coming soon

Certificates

Coming soon

Related Devices

Market Presence

Coming soon

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Uriki Test KOn Market