MOLECULIGHT I:X™
Mexico·Clase II·I. MEDICAL EQUIPMENT·SMITH & NEPHEW, S.A. DE C.V.·Registered July 16, 2019EL DISPOSITIVO AYUDA A LOS PROFESIONALES DE LA SALUD EN EL TRATAMIENTO DE PACIENTES CON HERIDAS AL PERMITIR LA VISUALIZACIÓN INSTANTÁNEA DE LA PRESENCIA DE BACTERIAS POTENCIALMENTE DAÑINAS COMÚNMENTE ENCONTRADAS EN O ALREDEDOR DE LAS HERIDAS, ENTRE LAS QU
THE DEVICE ASSISTS HEALTHCARE PROFESSIONALS IN THE TREATMENT OF WOUND PATIENTS BY ALLOWING INSTANT VISUALIZATION OF THE PRESENCE OF POTENTIALLY HARMFUL BACTERIA COMMONLY FOUND IN OR AROUND WOUNDS, AMONG WHICH
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- DISPOSITIVO PORTÁTIL GENERADOR DE IMÁGENES EN TIEMPO REAL DE LA CARGA BACTERIANA EN HERIDAS
- Trade Name (English)
- PORTABLE DEVICE THAT GENERATES REAL-TIME IMAGES OF BACTERIAL LOAD IN WOUNDS
- Analysis ID
- 1348E2019 SSA
- Registration Date
- July 16, 2019
- Name (Spanish)
- SMITH & NEPHEW, S.A. DE C.V.
- Name (English)
- SMITH & NEPHEW, S.A. DE C.V.
Access comprehensive regulatory information for MOLECULIGHT I:X™ (MOLECULIGHT I:X™) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1348E2019 SSA and manufactured by SMITH & NEPHEW, S.A. DE C.V.. The device was registered on July 16, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.