Terumo Destination Peripheral Guiding Sheath with CCV - FDA Registration CMDR-2022-00493A

Access comprehensive regulatory information for Terumo Destination Peripheral Guiding Sheath with CCV in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2022-00493A and manufactured by Terumo Medical Corporation - 265 Davidson Ave., Suite 320, Somerset, New Jersey USA mfd. By: Terumo Marketing Corporation - 950 Elkton Blvd. Elkton, Maryland, USA in USA. The device was registered on May 05, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Terumo Marketing Philippines, 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.