36429b43e8b153c7392d3cbb476d76f8

1. KAPA HYPEREXOME V2 PROBES

ROCHE SEQUENCING SOLUTIONS, INC·Colombia INVIMA·Expires November 01, 2033
Device classification
Product type (Spanish)
REACTIVOS IN VITRO
Product type (English)
REACTIVOS IN VITRO
Registration information
Analysis ID
36429b43e8b153c7392d3cbb476d76f8
Expire date
November 01, 2033
Authorized company / Fabricante
Name (English)
ROCHE SEQUENCING SOLUTIONS, INC
Product use / Uso del Producto
Spanish

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.

English

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.

About this record

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.