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Philippines FDA registration CMDR-2025-04930

Mindray Automated External Defibrillator

PhilippinesShenzhen Mindray Bio-Medical Electronics Co., Ltd. - Mindray Building, Keji 12th Road South, High-Tech Industrial Park, Nanshan, 518057 Shenzhen, People's Republic of China Mfd. by: Shenzhen Mindray Bio-Medical Electronics Co., Ltd. - 1203 Nanhuan Avenue, Guangming District, 518106 Shenzhen, People's Republic of ChinaChinaIssued June 26, 2025 – June 26, 2031
VerifiedFDA Philippines · official registry
Device information
Product Name
Mindray Automated External Defibrillator
Registration Number
CMDR-2025-04930
Manufacturer details
Country of Origin
China
Importer & distribution
Registration dates
Issuance Date
June 26, 2025
Expiry Date
June 26, 2031
About this record

Access comprehensive regulatory information for Mindray Automated External Defibrillator in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04930 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. - Mindray Building, Keji 12th Road South, High-Tech Industrial Park, Nanshan, 518057 Shenzhen, People's Republic of China Mfd. by: Shenzhen Mindray Bio-Medical Electronics Co., Ltd. - 1203 Nanhuan Avenue, Guangming District, 518106 Shenzhen, People's Republic of China in China. The device was registered on June 26, 2025.

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