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AMOYDX ROS1 GENE FUSIONS DETECTION KIT - INVIMA Registration 392580e5c293ac9a6bdb0c407aa1c0ec

Access comprehensive regulatory information for AMOYDX ROS1 GENE FUSIONS DETECTION KIT (AMOYDX ROS1 GENE FUSIONS DETECTION KIT ) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 392580e5c293ac9a6bdb0c407aa1c0ec and manufactured by EXOGENA LTDA.. The device was registered on January 02, 2027.

This page provides complete registration details including product type (DIAGNOSTIC REAGENT), 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
II
392580e5c293ac9a6bdb0c407aa1c0ec
AMOYDX ROS1 GENE FUSIONS DETECTION KIT
INVIMA Analysis ID: 392580e5c293ac9a6bdb0c407aa1c0ec
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS RELACIONADOS CON MUESTRAS PROCEDENTES DEL ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALYTES RELATED TO SAMPLES FROM THE HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
392580e5c293ac9a6bdb0c407aa1c0ec
Expire Date
January 02, 2027
Authorized Company / Fabricante
Name (Spanish)
EXOGENA LTDA.
Name (English)
EXOGENA LTDA.