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NEXTSEQ™ 2000 P3 REAGENTS - INVIMA Registration 4a74fd6c03ff3711204d77d441198375

Access comprehensive regulatory information for NEXTSEQ™ 2000 P3 REAGENTS (NEXTSEQ™ 2000 P3 REAGENTS) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 4a74fd6c03ff3711204d77d441198375 and manufactured by ILLUMINA COLOMBIA S.A.S.. The device was registered on February 14, 2033.

This page provides complete registration details including product type (REACTIVOS IN VITRO), 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
I
4a74fd6c03ff3711204d77d441198375
NEXTSEQ™ 2000 P3 REAGENTS
INVIMA Analysis ID: 4a74fd6c03ff3711204d77d441198375
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Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
4a74fd6c03ff3711204d77d441198375
Expire Date
February 14, 2033
Authorized Company / Fabricante
Name (English)
ILLUMINA COLOMBIA S.A.S.