VASCO+ - COFEPRIS Registration 885C2019 SSA
Access comprehensive regulatory information for VASCO+ (BASQUE+) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 885C2019 SSA and manufactured by ISA HEALTH, S.A DE C.V.. The device was registered on April 30, 2019.
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.
DISPOSITIVO QUE SE UTILIZA PARA LA INYECCIรN DE PRODUCTOS DE DIAGNรSTICO O TERAPรUTICOS.
A DEVICE USED FOR THE INJECTION OF DIAGNOSTIC OR THERAPEUTIC PRODUCTS.

