DUS® - COFEPRIS Registration 1057R2019 SSA
Access comprehensive regulatory information for DUS® (SO®) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1057R2019 SSA and manufactured by KANA UNDESA, S.A. DE C.V.. The device was registered on May 17, 2019.
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.
SON TIRAS REACTIVAS DE INMERSIÓN Y LECTURA PARA USO DE DIAGNÓSTICO IN VITRO, QUE SIRVEN PARA LA DETERMINACIÓN DE UROBILINÓGENOS, GLUCOSA, BILIRRUBINA, CETONAS, GRAVEDAD ESPECIFICA, SANGRE, PH, PROTEÍNA, NITRITO, LEUCOCITOS, ÁCIDO ASCÓRBICO EN LA ORINA. E
THEY ARE DIP AND READING TEST STRIPS FOR IN VITRO DIAGNOSTIC USE, WHICH SERVE FOR THE DETERMINATION OF UROBILINOGENS, GLUCOSE, BILIRUBIN, KETONES, SPECIFIC GRAVITY, BLOOD, PH, PROTEIN, NITRITE, LEUKOCYTES, ASCORBIC ACID IN URINE. And