Stryker Crossflow Integrated Arthroscopy Pump - FDA Registration CMDR-2025-04733

Access comprehensive regulatory information for Stryker Crossflow Integrated Arthroscopy Pump in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04733 and manufactured by Transmedic Pte Ltd - 5 Jalan Kilang Barat, 9th Floor Petro Centre, Singapore 159349 Mfd. By: Stryker Ireland Ltd., Instrument Division - Carrigtwohill Business & Technology Park, Carrigtwohill, Co Cork T45 HV12 Ireland Mfd. For: Stryker Instruments, a division of Stryker Corporation - 1941 Stryker Way, Portage, MI 49002, USA in Singapore. The device was registered on June 10, 2025.

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