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STANDARD™Q LEPTOSPIRA IGM/IGG TEST - INVIMA Registration 00252c08247b139c45975aeab230a7b3

Access comprehensive regulatory information for STANDARD™Q LEPTOSPIRA IGM/IGG TEST (STANDARD™Q LEPTOSPIRA IGM/IGG TEST) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 00252c08247b139c45975aeab230a7b3 and manufactured by QUIMIOLAB S.A.S.

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
III
00252c08247b139c45975aeab230a7b3
STANDARD™Q LEPTOSPIRA IGM/IGG TEST
INVIMA Analysis ID: 00252c08247b139c45975aeab230a7b3
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Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
00252c08247b139c45975aeab230a7b3
Authorized Company / Fabricante
Name (Spanish)
QUIMIOLAB S.A.S
Name (English)
QUIMIOLAB S.A.S