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Data last updated: Apr 2025

Integral

36633940135R2

On MarketClass I

RegulationEU MDR

Manufactureranthogyr

Primary DI03663394485500

ReferenceGTIWG50L

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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 DI03663394485500

Basic UDI-DI36633940135R2

ReferenceGTIWG50L

Issuing Agency—

ULIDN0M0ST8K

Classification

Risk ClassClass I

RegulationEU MDR

StatusOn Market

Device TypesComing soon

Manufacturer

Manufactureranthogyr

Manufacturer SRNFR-MF-000000602

Manufacturer StatusActive

CND Nomenclature

V0599CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER

Coming soon

Certificates

Coming soon

Related Devices

Market Presence

Coming soon