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RNASE P ASSAY (TAMRA) 440µL 200TEST - INVIMA Registration 8deb867c28fe1b7dbb30965003b14c64

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.

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INVIMA Official Data
I
8deb867c28fe1b7dbb30965003b14c64
RNASE P ASSAY (TAMRA) 440µL 200TEST
INVIMA Analysis ID: 8deb867c28fe1b7dbb30965003b14c64
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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

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 (English)
AM ASESORIA Y MANTENIMIENTO LTDA