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NEXTSEQ™ 1000/2000 READ PRIMER KIT - INVIMA Registration 21bb7feb5c85fb92f0f8c81af55fcef6

Access comprehensive regulatory information for NEXTSEQ™ 1000/2000 READ PRIMER KIT (NEXTSEQ™ 1000/2000 READ PRIMER KIT) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 21bb7feb5c85fb92f0f8c81af55fcef6 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
21bb7feb5c85fb92f0f8c81af55fcef6
NEXTSEQ™ 1000/2000 READ PRIMER KIT
INVIMA Analysis ID: 21bb7feb5c85fb92f0f8c81af55fcef6
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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
21bb7feb5c85fb92f0f8c81af55fcef6
Expire Date
February 14, 2033
Authorized Company / Fabricante
Name (English)
ILLUMINA COLOMBIA S.A.S.