f3c66a5f4329ec53523bf900b4f85553

CRP TEST KIT

INSTRUMENTACION S.A.·II·Colombia INVIMA·Expires May 05, 2031

Device classification

Risk class / Clase de Riesgo: II
Product type (Spanish): REACTIVO DIAGNOSTICO
Product type (English): DIAGNOSTIC REAGENT

Registration information

Analysis ID: f3c66a5f4329ec53523bf900b4f85553
Expire date: May 05, 2031

Authorized company / Fabricante

Name (Spanish): INSTRUMENTACION S.A.
Name (English): INSTRUMENTACION S.A.

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

About this record

Access comprehensive regulatory information for CRP TEST KIT (CRP TEST KIT) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID f3c66a5f4329ec53523bf900b4f85553 and manufactured by INSTRUMENTACION S.A.. The device was registered on May 05, 2031.

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.