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GEM® HEMOCHRON™ 100 ACTIVATED CLOTTING TIME PLUS TEST (ACT+) 000GACT+ - INVIMA Registration 401b52e39e8ead5278bb843f7e40267f

Access comprehensive regulatory information for GEM® HEMOCHRON™ 100 ACTIVATED CLOTTING TIME PLUS TEST (ACT+) 000GACT+ (GEM® HEMOCHRON™ 100 ACTIVATED CLOTTING TIME PLUS TEST (ACT+) 000GACT+) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 401b52e39e8ead5278bb843f7e40267f and manufactured by WERFEN COLOMBIA S.A.S. The device was registered on October 14, 2032.

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
401b52e39e8ead5278bb843f7e40267f
GEM® HEMOCHRON™ 100 ACTIVATED CLOTTING TIME PLUS TEST (ACT+) 000GACT+
INVIMA Analysis ID: 401b52e39e8ead5278bb843f7e40267f
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Product Use / Uso del Producto
Spanish

DETERMINACIÓN 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
401b52e39e8ead5278bb843f7e40267f
Expire Date
October 14, 2032
Authorized Company / Fabricante
Name (Spanish)
WERFEN COLOMBIA S.A.S
Name (English)
THROW COLOMBIA S.A.S