8089ec9b562b74bbcdc7f1428920391f

LIGHTMIX KIT DIGITAL KRAS G12D

ROCHE DIAGNOSTICS GMBH·I·Colombia INVIMA·Expires March 11, 2034

Device classification

Risk class / Clase de Riesgo: I
Product type (Spanish): REACTIVOS IN VITRO
Product type (English): REACTIVOS IN VITRO

Registration information

Analysis ID: 8089ec9b562b74bbcdc7f1428920391f
Expire date: March 11, 2034

Authorized company / Fabricante

Name (Spanish): ROCHE DIAGNOSTICS GMBH
Name (English): ROCHE DIAGNOSTICS GMBH

About this record

Access comprehensive regulatory information for LIGHTMIX KIT DIGITAL KRAS G12D (LIGHTMIX KIT DIGITAL KRAS G12D) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 8089ec9b562b74bbcdc7f1428920391f and manufactured by ROCHE DIAGNOSTICS GMBH. The device was registered on March 11, 2034.

This page provides complete registration details including product type (REACTIVOS IN VITRO), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.