e59deb37b6bdcb10b52e3d269ce15618

LIGHTMIX KIT DIGITAL EGFR_EX19DEL

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: e59deb37b6bdcb10b52e3d269ce15618
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 EGFR_EX19DEL (LIGHTMIX KIT DIGITAL EGFR_EX19DEL) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID e59deb37b6bdcb10b52e3d269ce15618 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.