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ALK-P80 (EP302) - INVIMA Registration 046d08f32c0d27fe3da79429f3146fe4

Access comprehensive regulatory information for ALK-P80 (EP302) ( ALK-P80 (EP302)) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 046d08f32c0d27fe3da79429f3146fe4 and manufactured by INMUNOTECH LABORATORIES S.A.S.. The device was registered on August 03, 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
046d08f32c0d27fe3da79429f3146fe4
ALK-P80 (EP302)
INVIMA Analysis ID: 046d08f32c0d27fe3da79429f3146fe4
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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
046d08f32c0d27fe3da79429f3146fe4
Expire Date
August 03, 2031
Authorized Company / Fabricante
Name (English)
INMUNOTECH LABORATORIES S.A.S.