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Data last updated: Apr 2025

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3760301940138G

On MarketClass I

RegulationEU MDR

ManufacturerNEWMEDI

Primary DI37603019401352

ReferenceERP013

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 DI37603019401352

Basic UDI-DI3760301940138G

ReferenceERP013

Issuing Agency—

ULIDRPZ2HXBW

Classification

Risk ClassClass I

RegulationEU MDR

StatusOn Market

Device TypesComing soon

Manufacturer

ManufacturerNEWMEDI

Manufacturer SRNFR-MF-000000922

Manufacturer StatusActive

CND Nomenclature

V0599CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER

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Certificates

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Related Devices

Market Presence

Coming soon

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