Inmed® Fingertip Pule Oximeter - FDA Registration CMDR-2025-03296

Access comprehensive regulatory information for Inmed® Fingertip Pule Oximeter in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03296 and manufactured by Shenzhen Aeon Technology Co., Ltd. RM6H02, Block 27-29, Tianxia IC Industrial Park, Majialong, No. 133 of Yiyuan Road, Natou Street, Nanshan District, 518052 Shenzhen, People's Republic of China MfdBy: Shenzhen Aeon Technology Co., Ltd. Bao'an Branch - 3/F, Block B, Bldg 6, Industrial Zone of Yusheng, No. 467 of 107 National Highway, Gushu Intersection, Xixiang Street, Bao-an District, 518126 Shenzhen, People's Republic of China in China. The device was registered on January 28, 2025.

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