DIRUI
LA SERIE H Y H-800 DIRUI DE TIRAS REACTIVAS SE EMPLEAN PARA EL ANÁLISIS CUALITATIVO Y SEMI-CUANTITATIVO DE UROBILINÓGENO, BILIRRUBINA, CETONA (ÁCIDO ACETO ACÉTICO), SANGRE, PROTEÍNAS, NITRITOS, LEUCOCITOS, GLUCOSA, GRAVEDAD ESPECIFICA, PH, ÁCIDO ASCÓRBICO
THE H AND H-800 DIRUI SERIES OF TEST STRIPS ARE USED FOR THE QUALITATIVE AND SEMI-QUANTITATIVE ANALYSIS OF UROBILINOGEN, BILIRUBIN, KETONE (ACETIC ACETIC ACID), BLOOD, PROTEINS, NITRITES, LEUKOCYTES, GLUCOSE, SPECIFIC GRAVITY, PH, ASCORBIC ACID
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- TIRAS REACTIVAS PARA URIANÁLISIS
- Trade Name (English)
- TEST STRIPS FOR URINALYSIS
- Analysis ID
- 616R2018 SSA
- Registration Date
- March 01, 2018
- Name (Spanish)
- DISTRIBUIDORA QUÍMICA INTEGRAL, S.A. DE C.V.
- Name (English)
- DISTRIBUIDORA QUÍMICA INTEGRAL, S.A. DE C.V.
Access comprehensive regulatory information for DIRUI (DIRUI) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 616R2018 SSA and manufactured by DISTRIBUIDORA QUÍMICA INTEGRAL, S.A. DE C.V.. The device was registered on March 01, 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.