3M AVAGARD FOAMING - COFEPRIS Registration 1950C2021 SSA
Access comprehensive regulatory information for 3M AVAGARD FOAMING (3M AVAGARD FOAMING) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1950C2021 SSA and manufactured by 3M MÉXICO, S.A. DE C.V.. The device was registered on November 24, 2021.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.
ESTÁ INDICADO PARA USO COMO UNANTISÉPTICO PARA MANOS, PARA ELCUIDADODELASALUDPERSONAL.REDUCELAS BACTERIAS QUE POTENCIALMENTEPUEDEN CAUSAR ENFERMEDADES
IT IS INDICATED FOR USE AS A HAND ANTISEPTIC, FOR PERSONAL HEALTH CARE. REDUCES BACTERIA THAT CAN POTENTIALLY CAUSE DISEASE