INTRAFIX® PRIMELINE I.S. LUER LOCK WITH Y-INJECTION SITE, STERILE - FDA Registration MDR-01900

Access comprehensive regulatory information for INTRAFIX® PRIMELINE I.S. LUER LOCK WITH Y-INJECTION SITE, STERILE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01900 and manufactured by B. Braun Melsungen AG in Vietnam. The device was registered on March 18, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (B. Braun Medical Supplies, 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.