17. KIT VIRTUAL KAPA STRANDED MRNA-SEQ KIT
- Risk class / Clase de Riesgo
- I
- Product type (Spanish)
- REACTIVOS IN VITRO
- Product type (English)
- REACTIVOS IN VITRO
- Analysis ID
- f8684694733c2d475015b386cca679db
- Expire date
- February 09, 2033
- Name (Spanish)
- ROCHE SEQUENCING SOLUTIONS, INC
- Name (English)
- ROCHE SEQUENCING SOLUTIONS, INC
LOS REACTIVOS RUO 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_x000D_ TECNOLÓGICA ES POR TECNICAS DE BIOLOGIA MOLECULAR POR AMPLIFICACIÓN EN CADENA DE POLIMERASA PCR.
THE RUO REAGENTS COVERED IN THIS SANITARY REGISTRY ARE REAGENTS FOR THE PREPARATION OF SAMPLES, AMPLIFICACION_x000D_ DETECTION AND / OR QUANTIFICATION IN BIOLOGICAL SAMPLES OF HUMAN ORIGIN, OF NUCLEIC ACIDS DNA / RNA. YOUR PLATAFORMA_x000D_ TECHNOLOGICAL IS BY MOLECULAR BIOLOGY TECHNIQUES BY PCR POLYMERASE CHAIN AMPLIFICATION.
Access comprehensive regulatory information for 17. KIT VIRTUAL KAPA STRANDED MRNA-SEQ KIT (17. KIT VIRTUAL KAPA STRANDED MRNA-SEQ KIT) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID f8684694733c2d475015b386cca679db and manufactured by ROCHE SEQUENCING SOLUTIONS, INC. The device was registered on February 09, 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.