B125M Patient Monitor System B125M with softare version VSP 3.0 - FDA Registration CMDR-2024-02807

Access comprehensive regulatory information for B125M Patient Monitor System B125M with softare version VSP 3.0 in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02807 and manufactured by GE Medical Systems Information Technologies, Inc. 9900 Innovation Drive Wauwatosa, WI 53226, USA Mfd By: GE Medical Systems (China) Co., Ltd. - No. 19, Changjiang Road, Wuxi National Hi-Tech Development Zone Jiangsu, P.R. China in USA. The device was registered on May 10, 2024.

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