NIOX VERO®
Mexico·Clase I·I. MEDICAL EQUIPMENT·MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.·Registered August 07, 2018NIOX VERO MIDE EL ÓXIDO NÍTRICO (NO) EN EL ALIENTO HUMANO.
NIOX VERO MEASURES NITRIC OXIDE (NO) IN HUMAN BREATH.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- MONITOR DE INFLAMACIÓN DE VÍAS RESPIRATORIAS
- Trade Name (English)
- AIRWAY INFLAMMATION MONITOR
- Analysis ID
- 1938E2018 SSA
- Registration Date
- August 07, 2018
- Name (Spanish)
- MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.
- Name (English)
- MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.
Access comprehensive regulatory information for NIOX VERO® (NIOX VERO®) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1938E2018 SSA and manufactured by MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.. The device was registered on August 07, 2018.
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.