PRUEBA DE EMBARAZO DIGITAL EN UN SOLO PASO
Mexico·Clase I·III. DIAGNOSTIC AGENTS·KABLA COMERCIAL, S.A. DE C.V.·Registered February 07, 2019PRUEBA RÁPIDA Y CUALITATIVA PARA LA DETERMINACIÓN DE GONADOTROPINA CORIÓNICA HUMANA (HCG) EN ORINA. ESTA PRUEBA ESTA INDICADA PARA EL AUTO-ANÁLISIS.
RAPID AND QUALITATIVE TEST FOR THE DETERMINATION OF HUMAN CHORIONIC GONADOTROPIN (HCG) IN URINE. THIS TEST IS INDICATED FOR SELF-ANALYSIS.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- PRUEBA RÁPIDA DIGITAL PARA LA DETECCIÓN CUALITATIVA DE LA HORMONA GONADOTROPINA CORIÓNICA HUMANA (HC
- Trade Name (English)
- DIGITAL RAPID TEST FOR THE QUALITATIVE DETECTION OF HUMAN CHORIONIC GONADOTROPIN HORMONE (HC
- Analysis ID
- 227R2019 SSA
- Registration Date
- February 07, 2019
- Name (Spanish)
- KABLA COMERCIAL, S.A. DE C.V.
- Name (English)
- KABLA COMERCIAL, S.A. DE C.V.
Access comprehensive regulatory information for PRUEBA DE EMBARAZO DIGITAL EN UN SOLO PASO (ONE-STEP DIGITAL PREGNANCY TEST) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 227R2019 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on February 07, 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.