BD MAX™ UVE SPECIMEN COLLECTION KIT
Mexico·Clase II·III. DIAGNOSTIC AGENTS·BECTON DICKINSON DE MÉXICO, S.A. DE C.V.·Registered August 09, 2018BD MAX UVE SPECIMEN COLLECTION KIT (KIT DE RECOLECCIÓN DE MUESTRAS BD MAX UVE) ESTÁ DISEÑADO PARA UTILIZARSE EN UN ENTORNO CLÍNICO DE ACUERDO CON LAS INSTRUCCIONES PROPORCIONADAS PARA LA RECOLECCIÓN Y EL TRANSPORTE DE MUESTRAS VAGINALES Y ENDOCERVICALES E
BD MAX UVE SPECIMEN COLLECTION KIT IS DESIGNED FOR USE IN A CLINICAL SETTING IN ACCORDANCE WITH THE INSTRUCTIONS PROVIDED FOR THE COLLECTION AND TRANSPORT OF VAGINAL AND ENDOCERVICAL SPECIMENS AND
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- KIT PARA RECOLECCIÓN DE MUESTRAS VAGINALES Y ENDOCERVICALES
- Trade Name (English)
- KIT FOR COLLECTION OF VAGINAL AND ENDOCERVICAL SAMPLES
- Analysis ID
- 1963R2018 SSA
- Registration Date
- August 09, 2018
- Name (Spanish)
- BECTON DICKINSON DE MÉXICO, S.A. DE C.V.
- Name (English)
- BECTON DICKINSON DE MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for BD MAX™ UVE SPECIMEN COLLECTION KIT (BD MAX™ UVE SPECIMEN COLLECTION KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1963R2018 SSA and manufactured by BECTON DICKINSON DE MÉXICO, S.A. DE C.V.. The device was registered on August 09, 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.