Bone Cutting and Drilling Devices- Stryker® Egg - FDA Registration CMDR-2025-05128

Access comprehensive regulatory information for Bone Cutting and Drilling Devices- Stryker® Egg in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-05128 and manufactured by Transmedic Pte Ltd. - 5 Jalan Kilang Barat, 9th Floor Petro Centre, Singapore 159349 Mfd by: Stryker Ireland Ltd. - Instruments 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 July 14, 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.