Medima Line ST12L Infusion Set - FDA Registration CMDR-2024-03290

Access comprehensive regulatory information for Medima Line ST12L Infusion Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03290 and manufactured by MEDIMA Sp. Z.o.o. - AI, Jerozolimskie 200, 02-466 Warsaw, Poland Mfd. By: BQ Plus Medical Co., Ltd. - No. 18, Cheye Road, Songjiang District, Shanghai 201611, China in China. The device was registered on October 03, 2024.

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