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LIGHTMIX KIT DIGITAL PIK3CA E545K - INVIMA Registration 8d81763a1d3c30b781c3eebb3be140e6

Access comprehensive regulatory information for LIGHTMIX KIT DIGITAL PIK3CA E545K (LIGHTMIX KIT DIGITAL PIK3CA E545K) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 8d81763a1d3c30b781c3eebb3be140e6 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.

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INVIMA Official Data
I
8d81763a1d3c30b781c3eebb3be140e6
LIGHTMIX KIT DIGITAL PIK3CA E545K
INVIMA Analysis ID: 8d81763a1d3c30b781c3eebb3be140e6
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Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
8d81763a1d3c30b781c3eebb3be140e6
Expire Date
March 11, 2034
Authorized Company / Fabricante
Name (English)
ROCHE DIAGNOSTICS GMBH