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STANDARD™Q SYPHILIS AB TEST - INVIMA Registration c4cd4d174612c1f37346ea3e71ec3fef

Access comprehensive regulatory information for STANDARD™Q SYPHILIS AB TEST (STANDARD™Q SYPHILIS AB TEST) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID c4cd4d174612c1f37346ea3e71ec3fef 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
c4cd4d174612c1f37346ea3e71ec3fef
STANDARD™Q SYPHILIS AB TEST
INVIMA Analysis ID: c4cd4d174612c1f37346ea3e71ec3fef
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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
c4cd4d174612c1f37346ea3e71ec3fef
Authorized Company / Fabricante
Name (Spanish)
QUIMIOLAB S.A.S
Name (English)
QUIMIOLAB S.A.S