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QUANTA FLASH® HMGCR REAGENTS - INVIMA Registration 50c65dffc69c0c05f974cb7e627126e9

Access comprehensive regulatory information for QUANTA FLASH® HMGCR REAGENTS (QUANTA FLASH® HMGCR REAGENTS) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID 50c65dffc69c0c05f974cb7e627126e9 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
50c65dffc69c0c05f974cb7e627126e9
QUANTA FLASH® HMGCR REAGENTS
INVIMA Analysis ID: 50c65dffc69c0c05f974cb7e627126e9
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Device Classification
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
50c65dffc69c0c05f974cb7e627126e9
Expire Date
September 09, 2031
Authorized Company / Fabricante
Name (Spanish)
WERFEN COLOMBIA S.A.S
Name (English)
THROW COLOMBIA S.A.S