Suru Cenocath® Double Lumen Central Venous Catheter Kit - FDA Registration CMDR-2025-03826B

Access comprehensive regulatory information for Suru Cenocath® Double Lumen Central Venous Catheter Kit in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03826B and manufactured by SURU International Pvt., Limited in India. The device was registered on February 04, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Iraseth Pharma 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.