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DDPCR CNV ASSAY (HEX), 200X20µL REACTIONS - INVIMA Registration 624b026c7b00aa46d8f4d2e9fa9e8739

Access comprehensive regulatory information for DDPCR CNV ASSAY (HEX), 200X20µL REACTIONS (DDPCR CNV ASSAY (HEX), 200X20µL REACTIONS) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 624b026c7b00aa46d8f4d2e9fa9e8739 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
624b026c7b00aa46d8f4d2e9fa9e8739
DDPCR CNV ASSAY (HEX), 200X20µL REACTIONS
INVIMA Analysis ID: 624b026c7b00aa46d8f4d2e9fa9e8739
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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
624b026c7b00aa46d8f4d2e9fa9e8739
Expire Date
April 25, 2032
Authorized Company / Fabricante
Name (English)
AM ASESORIA Y MANTENIMIENTO LTDA