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QUIDEL TRIAGETRUE™ HIGH SENSITIVITY TROPONIN I TEST - INVIMA Registration 1ede6f7e5bb2c890f2a01dbf1f546eb5

Access comprehensive regulatory information for QUIDEL TRIAGETRUE™ HIGH SENSITIVITY TROPONIN I TEST (QUIDEL TRIAGETRUE™ HIGH SENSITIVITY TROPONIN I TEST) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 1ede6f7e5bb2c890f2a01dbf1f546eb5 and manufactured by ORTHO-CLINICAL DIAGNOSTICS COLOMBIA S.A.S. The device was registered on February 05, 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
1ede6f7e5bb2c890f2a01dbf1f546eb5
QUIDEL TRIAGETRUE™ HIGH SENSITIVITY TROPONIN I TEST
INVIMA Analysis ID: 1ede6f7e5bb2c890f2a01dbf1f546eb5
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Product Use / Uso del Producto
Spanish

DETERMINACIÓN DE LOS DIFERENTES ANALITOS_x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL_x000D_ ORGANISMO HUMAN0.

English

DETERMINATION OF THE DIFFERENT ANALITOS_x000D_ RELATED TO SAMPLES FROM DEL_x000D_ HUMAN ORGANISM0.

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
1ede6f7e5bb2c890f2a01dbf1f546eb5
Expire Date
February 05, 2034
Authorized Company / Fabricante
Name (English)
ORTHO-CLINICAL DIAGNOSTICS COLOMBIA S.A.S