URITOP + BIOSYNEX® - COFEPRIS Registration 2473R2018 SSA
Access comprehensive regulatory information for URITOP + BIOSYNEX® (URITOP + BIOSYNEX®) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2473R2018 SSA and manufactured by PHARMACUR, S.A. DE C.V.. The device was registered on October 26, 2018.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
LAS TIRAS REACTIVAS PARA ANÁLISIS DE ORINA URITOP+ ESTÁN DESTINADAS PARA LA DETECCIÓN CUALITATIVA Y SEMI-CUANTITATIVA EN ORINA HUMANA DE UNO O MÁS PARÁMETROS: UROBILINÓGENO, GLUCOSA, BILIRRUBINA, CETONAS (ÁCIDO ACETOACÉTICO), GRAVEDAD ESPECÍFICA, SANGRE,
URITOP+ URINALYSIS TEST STRIPS ARE INTENDED FOR THE QUALITATIVE AND SEMI-QUANTITATIVE DETECTION IN HUMAN URINE OF ONE OR MORE PARAMETERS: UROBILINOGEN, GLUCOSE, BILIRUBIN, KETONES (ACETOACETIC ACID), SPECIFIC GRAVITY, BLOOD,