0a793283bf572d47adaf2044177e9eaa

TOXO IGM CLIA MICROPARTICLES

BIOLORE LTDA.·II·Colombia INVIMA·Expires June 15, 2031
Device classification
Risk class / Clase de Riesgo
II
Product type (Spanish)
REACTIVO DIAGNOSTICO
Product type (English)
DIAGNOSTIC REAGENT
Registration information
Analysis ID
0a793283bf572d47adaf2044177e9eaa
Expire date
June 15, 2031
Authorized company / Fabricante
Name (Spanish)
BIOLORE LTDA.
Name (English)
BIOLORE LTDA.
Product use / Uso del Producto
Spanish

ESTE ENSAYO SE BASA EN UN INMUNOENSAYO DE MICROPARTÍCULAS QUIMILUMINISCENTES (MICROPARTÍCULAS CLIA) PARA LA DETERMINACION CUANTITATIVA DE TOXO IGM (ANTICUERPOS IGM CONTRA TOXOPLASMA GONDII) EN SUERO O PLASMA HUMANO. _x000D_

English

THIS ASSAY IS BASED ON AN IMMUNOASSAY OF CHEMILUMINESCENT MICROPARTICLES (CLIA MICROPARTICLES) FOR THE QUANTITATIVE DETERMINATION OF IGM TOXO (IGM ANTIBODIES AGAINST TOXOPLASMA GONDII) IN HUMAN SERUM OR PLASMA. _x000D_

About this record

Access comprehensive regulatory information for TOXO IGM CLIA MICROPARTICLES (TOXO IGM CLIA MICROPARTICLES) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 0a793283bf572d47adaf2044177e9eaa and manufactured by BIOLORE LTDA.. The device was registered on June 15, 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.