a92656c0f44a5372e1b3d8a6f6eba119

TSO 500 DNA/RNA + 3 NEXTSEQ HO FC

ILLUMINA COLOMBIA S.A.S.·Colombia INVIMA·Expires October 17, 2033
Device classification
Product type (Spanish)
REACTIVOS IN VITRO
Product type (English)
REACTIVOS IN VITRO
Registration information
Analysis ID
a92656c0f44a5372e1b3d8a6f6eba119
Expire date
October 17, 2033
Authorized company / Fabricante
Name (English)
ILLUMINA COLOMBIA S.A.S.
Product use / Uso del Producto
Spanish

REACTIVOS DE BIOLOGÍA MOLECULAR USADOS PARA LA_x000D_ PREPARACIÓN DE BIBLIOTECAS DE FRAGMENTOS DE _x000D_ ÁCIDOS NUCLEICOS DIRIGIDAS A PROCESOS DE_x000D_ SECUENCIACIÓN DE PRÓXIMA GENERACIÓN Y DE CAPTURA _x000D_ HÍBRIDA, PARA LA IDENTIFICACIÓN DE VARIANTES _x000D_ GENÉTICAS. PARA USO EXCLUSIVO EN INVESTIGACIÓN, _x000D_ "RESEARCH USE ONLY" "RUO".

English

MOLECULAR BIOLOGY REAGENTS USED FOR LA_x000D_ PREPARING _x000D_ FRAGMENT LIBRARIES NUCLEIC ACIDS TARGETING DE_x000D_ PROCESSES NEXT-GENERATION AND CAPTURE SEQUENCING _x000D_ HYBRID, FOR THE IDENTIFICATION OF _x000D_ VARIANTS GENETIC. FOR RESEARCH USE ONLY, _x000D_ "RESEARCH USE ONLY" "RUO".

About this record

Access comprehensive regulatory information for TSO 500 DNA/RNA + 3 NEXTSEQ HO FC (TSO 500 DNA/RNA + 3 NEXTSEQ HO FC) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID a92656c0f44a5372e1b3d8a6f6eba119 and manufactured by ILLUMINA COLOMBIA S.A.S.. The device was registered on October 17, 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.