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ESTRADIOL ELISA - INVIMA Registration d5a29b80df197dae9e4593c6897fe46d

Access comprehensive regulatory information for ESTRADIOL ELISA (ESTRADIOL ELISA) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID d5a29b80df197dae9e4593c6897fe46d and manufactured by BIOLORE LTDA.. The device was registered on April 25, 2032.

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
d5a29b80df197dae9e4593c6897fe46d
ESTRADIOL ELISA
INVIMA Analysis ID: d5a29b80df197dae9e4593c6897fe46d
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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
d5a29b80df197dae9e4593c6897fe46d
Expire Date
April 25, 2032
Authorized Company / Fabricante
Name (Spanish)
BIOLORE LTDA.
Name (English)
BIOLORE LTDA.