SMARTSITE® 20mm VENTED VIAL ACCESS DEVICE WITH 0.2 MICRON HYDROPHOBIC AIR-VENTING FILTER - FDA Registration MDR-04869

Access comprehensive regulatory information for SMARTSITE® 20mm VENTED VIAL ACCESS DEVICE WITH 0.2 MICRON HYDROPHOBIC AIR-VENTING FILTER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04869 and manufactured by Carefusion Switzerland 317 Sarl in Switzerland. The device was registered on November 07, 2017.

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