ec86f1588b8541f78c53eaf5fa12bb79

ONSITE H.PYLORI AG RAPID TEST

BIOLORE LTDA·II·Colombia INVIMA·Expires March 05, 2034

Device classification

Risk class / Clase de Riesgo: II
Product type (Spanish): REACTIVO DIAGNOSTICO
Product type (English): DIAGNOSTIC REAGENT

Registration information

Analysis ID: ec86f1588b8541f78c53eaf5fa12bb79
Expire date: March 05, 2034

Authorized company / Fabricante

Name (Spanish): BIOLORE LTDA
Name (English): BIOLORE LTDA

Product use / Uso del Producto

Spanish

INMUNOENSAYO CROMATOGRAFICO DE FLUJO LATERAL PARA LA DETECCION CUALITATIVA DEL ANTIGENO H. PYLORI EN SUERO O PLASMA

English

LATERAL FLOW CHROMATOGRAPHIC IMMUNOASSAY FOR THE QUALITATIVE DETECTION OF H. PYLORI ANTIGEN IN SERUM OR PLASMA

About this record

Access comprehensive regulatory information for ONSITE H.PYLORI AG RAPID TEST (ONSITE H.PYLORI AG RAPID TEST) in the Colombia medical device market through Pure Global AI's free database. This II medical device is registered under INVIMA analysis ID ec86f1588b8541f78c53eaf5fa12bb79 and manufactured by BIOLORE LTDA. The device was registered on March 05, 2034.

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.