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CYSTAIN?™ PI ABSOLUTE P - INVIMA Registration b7c9352cbacffcf60652175ef45ef354

Access comprehensive regulatory information for CYSTAIN?™ PI ABSOLUTE P (CYSTAIN?™ PI ABSOLUTE P) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID b7c9352cbacffcf60652175ef45ef354 and manufactured by SYSMEX COLOMBIA S.A.S. The device was registered on October 14, 2031.

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
b7c9352cbacffcf60652175ef45ef354
CYSTAIN?™ PI ABSOLUTE P
INVIMA Analysis ID: b7c9352cbacffcf60652175ef45ef354
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Product Use / Uso del Producto
Spanish

PARA USO EXCLUSIVO EN INVESTIGACIÓN. NO PARA USO EN PROCEDIMIENTOS DE DIAGNÓSTICO.

English

FOR USE IN RESEARCH ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES.

Device Classification
Risk Class / Clase de Riesgo
I
Product Type (Spanish)
REACTIVOS IN VITRO
Product Type (English)
REACTIVOS IN VITRO
Registration Information
Analysis ID
b7c9352cbacffcf60652175ef45ef354
Expire Date
October 14, 2031
Authorized Company / Fabricante
Name (Spanish)
SYSMEX COLOMBIA S.A.S
Name (English)
SYSMEX COLOMBIA S.A.S