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QUANTA FLASH® DGP IGG REAGENTS - INVIMA Registration ddd44f3a8bc0307f3c20e4f6b4fa6907

Access comprehensive regulatory information for QUANTA FLASH® DGP IGG REAGENTS (QUANTA FLASH® DGP IGG REAGENTS) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID ddd44f3a8bc0307f3c20e4f6b4fa6907 and manufactured by WERFEN COLOMBIA S.A.S. The device was registered on September 09, 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
ddd44f3a8bc0307f3c20e4f6b4fa6907
QUANTA FLASH® DGP IGG REAGENTS
INVIMA Analysis ID: ddd44f3a8bc0307f3c20e4f6b4fa6907
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Device Classification
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
ddd44f3a8bc0307f3c20e4f6b4fa6907
Expire Date
September 09, 2031
Authorized Company / Fabricante
Name (Spanish)
WERFEN COLOMBIA S.A.S
Name (English)
THROW COLOMBIA S.A.S