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1. DETECTION KIT FOR NONINVASIVE FETAL TRISOMY (T21, T18, T13) TEST (COMBINATORIAL PROBE-ANCHOR SYNTHESIS SEQUENCING METHOD) - INVIMA Registration d9b8f213a93f9d6dd489cb64103bfb92

Access comprehensive regulatory information for 1. DETECTION KIT FOR NONINVASIVE FETAL TRISOMY (T21, T18, T13) TEST (COMBINATORIAL PROBE-ANCHOR SYNTHESIS SEQUENCING METHOD) (1. DETECTION KIT FOR NONINVASIVE FETAL TRISOMY (T21, T18, T13) TEST (COMBINATORIAL PROBE-ANCHOR SYNTHESIS SEQUENCING METHOD)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID d9b8f213a93f9d6dd489cb64103bfb92 and manufactured by GENCELL PHARMA SAS. The device was registered on March 01, 2034.

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
d9b8f213a93f9d6dd489cb64103bfb92
1. DETECTION KIT FOR NONINVASIVE FETAL TRISOMY (T21, T18, T13) TEST (COMBINATORIAL PROBE-ANCHOR SYNTHESIS SEQUENCING METHOD)
INVIMA Analysis ID: d9b8f213a93f9d6dd489cb64103bfb92
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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
d9b8f213a93f9d6dd489cb64103bfb92
Expire Date
March 01, 2034
Authorized Company / Fabricante
Name (Spanish)
GENCELL PHARMA SAS
Name (English)
GENCELL PHARMA SAS