Stryker® Crossflow® Integrated Cassette Tubing - FDA Registration MDR-08079C

Access comprehensive regulatory information for Stryker® Crossflow® Integrated Cassette Tubing in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08079C and manufactured by Transmedic Pte Ltd.- 5 Jalan Kilang Barat, 9th Floor Petro Centre, Singapore 159349 mfd by: Infus Medical (Thailand) Co., Ltd.- 706 moo 4, Bangpoo Industrial Estate I-EA-T Free Zone, Tambon Preaksa Amphoe Muang Samutprakarn Samutprakam Province 10280 Thailand mfd for: Stryker Endoscopy, a Division of Stryker Corporation, also doing business as Stryker Endoscopy - 5900 Optical Court San Jose CA 95138 USA in USA. The device was registered on July 17, 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.