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Philippines FDA registration CMDR-2025-04949

Medcaptain Spirometer

PhilippinesMedcaptain Medical Technology Co., Ltd. - 12th Floor, Baiwang Research Building, No. 5158 Shahe West Road, Xili, Nanshan 518055 Shenzhen, Guangdong, China Mfd. by: Medcaptain Medical Technology Co., Ltd. - Building C, Jiale Science and Technology Industrial Park, Matian Street, Guangming, 518106 Shenzhen, Guangdong, ChinaChinaIssued June 24, 2025 – June 24, 2030
VerifiedFDA Philippines · official registry
Device information
Product Name
Medcaptain Spirometer
Registration Number
CMDR-2025-04949
Manufacturer details
Manufacturer
Medcaptain Medical Technology Co., Ltd. - 12th Floor, Baiwang Research Building, No. 5158 Shahe West Road, Xili, Nanshan 518055 Shenzhen, Guangdong, China Mfd. by: Medcaptain Medical Technology Co., Ltd. - Building C, Jiale Science and Technology Industrial Park, Matian Street, Guangming, 518106 Shenzhen, Guangdong, China
Country of Origin
China
Importer & distribution
Importer/Distributor
Biosite Medical Instrments
Registration dates
Issuance Date
June 24, 2025
Expiry Date
June 24, 2030
About this record

Access comprehensive regulatory information for Medcaptain Spirometer in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04949 and manufactured by Medcaptain Medical Technology Co., Ltd. - 12th Floor, Baiwang Research Building, No. 5158 Shahe West Road, Xili, Nanshan 518055 Shenzhen, Guangdong, China Mfd. by: Medcaptain Medical Technology Co., Ltd. - Building C, Jiale Science and Technology Industrial Park, Matian Street, Guangming, 518106 Shenzhen, Guangdong, China in China. The device was registered on June 24, 2025.

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