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CA 15-3 ELISA - INVIMA Registration 266185b00bc2519e428291c8cbbdbd67

Access comprehensive regulatory information for CA 15-3 ELISA (CA 15-3 ELISA) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 266185b00bc2519e428291c8cbbdbd67 and manufactured by BYO COLOMBIA S.A.S.. The device was registered on August 11, 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.

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INVIMA Official Data
II
266185b00bc2519e428291c8cbbdbd67
CA 15-3 ELISA
INVIMA Analysis ID: 266185b00bc2519e428291c8cbbdbd67
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N 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
266185b00bc2519e428291c8cbbdbd67
Expire Date
August 11, 2031
Authorized Company / Fabricante
Name (Spanish)
BYO COLOMBIA S.A.S.
Name (English)
BYO COLOMBIA S.A.S.