InnoQ ResFlow Disposable Laryngeal Mask Airway, PVC - FDA Registration CMDR-2025-04992

Access comprehensive regulatory information for InnoQ ResFlow Disposable Laryngeal Mask Airway, PVC in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04992 and manufactured by Global SCP Medical Systems Pte Ltd. - 1 Kallang Junction, Vanguard Campus #05-01, Singapore 339263 Mfd. By: Well Lead Medical Co., Ltd. - C-4 Jinhu Industrial Estate, Hualong 511434 Panyu, Guangzhou People's Republic of China in Singapore. The device was registered on July 09, 2025.

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