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LIGHTMIX KIT DIGITAL BRAF V600E - INVIMA Registration 16bd9688a915455c80efa29e81afeb95

Access comprehensive regulatory information for LIGHTMIX KIT DIGITAL BRAF V600E (LIGHTMIX KIT DIGITAL BRAF V600E) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 16bd9688a915455c80efa29e81afeb95 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
16bd9688a915455c80efa29e81afeb95
LIGHTMIX KIT DIGITAL BRAF V600E
INVIMA Analysis ID: 16bd9688a915455c80efa29e81afeb95
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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
16bd9688a915455c80efa29e81afeb95
Expire Date
March 11, 2034
Authorized Company / Fabricante
Name (English)
ROCHE DIAGNOSTICS GMBH