PORTEX THORACIC CATHETER, STRAGHT RADIO-OPAQUE - FDA Registration DVR-3688

Access comprehensive regulatory information for PORTEX THORACIC CATHETER, STRAGHT RADIO-OPAQUE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-3688 and manufactured by Smith Medical Instrument, Ltd. in Mexico. The device was registered on August 15, 2019.

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