STANDARD™ E TB-FERON ELISA - INVIMA Registration a5f2deeec569ea36340f4b0a53eaf8b5
Access comprehensive regulatory information for STANDARD™ E TB-FERON ELISA (STANDARD™ E TB-FERON ELISA) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID a5f2deeec569ea36340f4b0a53eaf8b5 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
a5f2deeec569ea36340f4b0a53eaf8b5
STANDARD™ E TB-FERON ELISA
INVIMA Analysis ID: a5f2deeec569ea36340f4b0a53eaf8b5
Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
a5f2deeec569ea36340f4b0a53eaf8b5
Authorized Company / Fabricante
Name (Spanish)
QUIMIOLAB S.A.SName (English)
QUIMIOLAB S.A.S

