Pure Global

HISOPO PARA RECOLECCIÓN DE MUESTRA VAGINAL - COFEPRIS Registration 1468R2024 SSA

Access comprehensive regulatory information for HISOPO PARA RECOLECCIÓN DE MUESTRA VAGINAL (HISOPO PARA RECOLECCIÓN DE MUESTRA VAGINAL) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1468R2024 SSA and manufactured by BECTON DICKINSON DE MÉXICO, S.A. DE C.V.. The device was registered on May 21, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.

Free Database
Powered by Pure Global AI
COFEPRIS Official Data
Clase II
1468R2024 SSA
HISOPO PARA RECOLECCIÓN DE MUESTRA VAGINAL
COFEPRIS Analysis ID: 1468R2024 SSA
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
SELF-FLOQSWABS® SELF- VAGINAL SWAB
Trade Name (English)
SELF-FLOQSWABS® SELF- VAGINAL SWAB
Registration Information
Analysis ID
1468R2024 SSA
Registration Date
May 21, 2024
Manufacturer / Fabricante
Name (English)
BECTON DICKINSON DE MÉXICO, S.A. DE C.V.