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Data last updated: Apr 2025

Uriki Test K

B-03770027558033

On MarketUnknown

RegulationEU MDR

ManufacturerIki

Primary DI03770027558033

ReferenceUT-K

View on EUDAMED

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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 DI03770027558033

Basic UDI-DIB-03770027558033

ReferenceUT-K

Issuing Agency—

ULID602C0RWQ

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

My UrikiOn Market

URIKI BOARDOn Market