Pure Global

ADENOVIRUS AND RSV COMBO RAPID TEST CASSETTE (NASOPHARYNGEAL SWAB) - COMBO PRUEBA RÁPIDA DE ADENOVIRUS Y RSV EN CASETE (HISOPOS NASOFARÍNGEOS) MARCA: ALL TEST - INVIMA Registration 3bd561ce64d8cdfcd80ff98ae0d087bb

Access comprehensive regulatory information for ADENOVIRUS AND RSV COMBO RAPID TEST CASSETTE (NASOPHARYNGEAL SWAB) - COMBO PRUEBA RÁPIDA DE ADENOVIRUS Y RSV EN CASETE (HISOPOS NASOFARÍNGEOS) MARCA: ALL TEST (ADENOVIRUS AND RSV COMBO RAPID TEST CASSETTE (NASOPHARYNGEAL SWAB) - COMBO PRUEBA RÁPIDA DE ADENOVIRUS Y RSV EN CASETE (HISOPOS NASOFARÍNGEOS) MARCA: ALL TEST) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID 3bd561ce64d8cdfcd80ff98ae0d087bb and manufactured by BIOLORE LTDA.. The device was registered on October 17, 2033.

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.

Free Database
Powered by Pure Global AI
INVIMA Official Data
II
3bd561ce64d8cdfcd80ff98ae0d087bb
ADENOVIRUS AND RSV COMBO RAPID TEST CASSETTE (NASOPHARYNGEAL SWAB) - COMBO PRUEBA RÁPIDA DE ADENOVIRUS Y RSV EN CASETE (HISOPOS NASOFARÍNGEOS) MARCA: ALL TEST
INVIMA Analysis ID: 3bd561ce64d8cdfcd80ff98ae0d087bb
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

DETERMINACIÓN DE LOS DIFERENTES ANALITOS _x000D_ RELACIONADOS CON MUESTRAS PROCEDENTES DEL _x000D_ ORGANISMO HUMANO.

English

DETERMINATION OF THE DIFFERENT ANALYTES _x000D_ RELATED TO SAMPLES FROM THE _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
3bd561ce64d8cdfcd80ff98ae0d087bb
Expire Date
October 17, 2033
Authorized Company / Fabricante
Name (Spanish)
BIOLORE LTDA.
Name (English)
BIOLORE LTDA.