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CYSTAIN™ PI ABSOLUTE P - INVIMA Registration 590e1618de56f558c6b57bf1217aaa61

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 590e1618de56f558c6b57bf1217aaa61 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
590e1618de56f558c6b57bf1217aaa61
CYSTAIN™ PI ABSOLUTE P
INVIMA Analysis ID: 590e1618de56f558c6b57bf1217aaa61
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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
590e1618de56f558c6b57bf1217aaa61
Expire Date
October 14, 2031
Authorized Company / Fabricante
Name (Spanish)
SYSMEX COLOMBIA S.A.S
Name (English)
SYSMEX COLOMBIA S.A.S