8deb867c28fe1b7dbb30965003b14c64

RNASE P ASSAY (TAMRA) 440µL 200TEST

AM ASESORIA Y MANTENIMIENTO LTDA·I·Colombia INVIMA·Expires April 25, 2032

Device classification

Risk class / Clase de Riesgo: I
Product type (Spanish): REACTIVOS IN VITRO
Product type (English): REACTIVOS IN VITRO

Registration information

Analysis ID: 8deb867c28fe1b7dbb30965003b14c64
Expire date: April 25, 2032

Authorized company / Fabricante

Name (Spanish): AM ASESORIA Y MANTENIMIENTO LTDA
Name (English): AM ASESORIA Y MANTENIMIENTO LTDA

Product use / Uso del Producto

Spanish

REACTIVOS UE PERMITEN AMPLIFICACION DE MUESTRAS MEDIANTE PCR EN TIEMPO REAL

English

UE REAGENTS ALLOW SAMPLE AMPLIFICATION BY REAL-TIME PCR

About this record

Access comprehensive regulatory information for RNASE P ASSAY (TAMRA) 440µL 200TEST (RNASE P ASSAY (TAMRA) 440µL 200TEST) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 8deb867c28fe1b7dbb30965003b14c64 and manufactured by AM ASESORIA Y MANTENIMIENTO LTDA. The device was registered on April 25, 2032.

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.