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HGH ELISA - INVIMA Registration 2fbfaf3621ca7ac07ec84dbd3684e5b0

Access comprehensive regulatory information for HGH ELISA (HGH ELISA) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 2fbfaf3621ca7ac07ec84dbd3684e5b0 and manufactured by BIOLORE LTDA. The device was registered on September 15, 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
2fbfaf3621ca7ac07ec84dbd3684e5b0
HGH ELISA
INVIMA Analysis ID: 2fbfaf3621ca7ac07ec84dbd3684e5b0
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Product Use / Uso del Producto
Spanish

DETERMINACIร“N DE LOS DIFERENTES ANALITOS _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES _x000D_ ORGANISMO HUMANO

English

DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM _x000D_ HUMAN ORGANISM

Device Classification
Risk Class / Clase de Riesgo
II
Product Type (Spanish)
REACTIVO DIAGNOSTICO
Product Type (English)
DIAGNOSTIC REAGENT
Registration Information
Analysis ID
2fbfaf3621ca7ac07ec84dbd3684e5b0
Expire Date
September 15, 2032
Authorized Company / Fabricante
Name (Spanish)
BIOLORE LTDA
Name (English)
BIOLORE LTDA