TACTICATH™ SENSORE ENABLED™ Contact Forece Ablation Catheter (Bi-Directional Handle) - FDA Registration CMDR-2022-00111B

Access comprehensive regulatory information for TACTICATH™ SENSORE ENABLED™ Contact Forece Ablation Catheter (Bi-Directional Handle) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2022-00111B and manufactured by Abbott Medical (Singapore) Pte., Ltd formerly St. Jude Medical (Singapore) Pte., Ltd. - Singapore. Mfd By: St. Jude Costa Rica LTDA. Alajuela, Costa Rica for: Abbott Medical - Plymouth, MN, USA in Singapore. The device was registered on February 11, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Biodevices, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.