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CK-MB/CTNI FAST TEST KIT(IMMUNOFLUORESCENCE ASSAY) - INVIMA Registration 17941662f8acc748d25c3efb8f9ae80a

Access comprehensive regulatory information for CK-MB/CTNI FAST TEST KIT(IMMUNOFLUORESCENCE ASSAY) (CK-MB/CTNI FAST TEST KIT(IMMUNOFLUORESCENCE ASSAY)) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID 17941662f8acc748d25c3efb8f9ae80a 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
17941662f8acc748d25c3efb8f9ae80a
CK-MB/CTNI FAST TEST KIT(IMMUNOFLUORESCENCE ASSAY)
INVIMA Analysis ID: 17941662f8acc748d25c3efb8f9ae80a
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Device Classification
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
17941662f8acc748d25c3efb8f9ae80a
Expire Date
November 11, 2031
Authorized Company / Fabricante
Name (English)
MARKETER OF PRODUCTS FOR LABORATORIES S.A.S., COMPROLAB S.A.S