1. KAPA HYPEREXOME V2 PROBES - INVIMA Registration 36429b43e8b153c7392d3cbb476d76f8
Access comprehensive regulatory information for 1. KAPA HYPEREXOME V2 PROBES (1. KAPA HYPEREXOME V2 PROBES) in the Colombia medical device market through Pure Global AI's free database. This medical device is registered under INVIMA analysis ID 36429b43e8b153c7392d3cbb476d76f8 and manufactured by ROCHE SEQUENCING SOLUTIONS, INC. The device was registered on November 01, 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.
LOS REACTIVOS RUO KAPA, AMPARADOS EN ES ESTE REGISTRO SANITARIO SON REACTIVOS PARA LA PREPARACION DE MUESTRAS, AMPLIFICACION _x000D_ DETECCIÒN Y/O CUANTIFICACIÓN EN MUESTRAS BIOLOGICAS DE ORIGEN HUMANO, DE LOS ACIDOS NUCLÉICOS DNA/RNA. SU PLATAFORMA TECNOLÓGICA _x000D_ ES POR TECNICAS DE BIOLOGIA MOLECULAR POR AMPLIFICACIÓN EN CADENA DE POLIMERASA PCR.
THE RUO KAPA REAGENTS, COVERED BY THIS SANITARY REGISTRY, ARE REAGENTS FOR THE PREPARATION OF SAMPLES, AMPLIFICATION _x000D_ DETECTION AND/OR QUANTIFICATION OF DNA/RNA NUCLEIC ACIDS IN BIOLOGICAL SAMPLES OF HUMAN ORIGIN. ITS _x000D_ TECHNOLOGY PLATFORM IT IS BY MOLECULAR BIOLOGY TECHNIQUES BY PCR POLYMERASE CHAIN AMPLIFICATION.