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CK-MB/CTNI CONTROL - INVIMA Registration dcbcf68f224a90ba2ec0137c3e81a04f

Access comprehensive regulatory information for CK-MB/CTNI CONTROL (CK-MB/CTNI CONTROL) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID dcbcf68f224a90ba2ec0137c3e81a04f and manufactured by COMERCIALIZADORA DE PRODUCTOS PARA LABORATORIOS S.A.S., COMPROLAB S.A.S. The device was registered on November 11, 2031.

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), 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
dcbcf68f224a90ba2ec0137c3e81a04f
CK-MB/CTNI CONTROL
INVIMA Analysis ID: dcbcf68f224a90ba2ec0137c3e81a04f
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Device Classification
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
dcbcf68f224a90ba2ec0137c3e81a04f
Expire Date
November 11, 2031
Authorized Company / Fabricante
Name (English)
MARKETER OF PRODUCTS FOR LABORATORIES S.A.S., COMPROLAB S.A.S