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ONSITE H.PYLORI AG RAPID TEST - INVIMA Registration ec86f1588b8541f78c53eaf5fa12bb79

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.

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INVIMA Official Data
II
ec86f1588b8541f78c53eaf5fa12bb79
ONSITE H.PYLORI AG RAPID TEST
INVIMA Analysis ID: ec86f1588b8541f78c53eaf5fa12bb79
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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

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