Philippines FDA registration CMDR-2025-04122

Comen Electrocardiograph

Name: Comen Electrocardiograph — Philippines FDA registration CMDR-2025-04122
Creator: Shenzhen Comen Medical Instruments Co., Ltd. - Floor 10, Floor 11 and Section C of Floor 12 of Building 1A 7 Floor 1 to Floor 5 of Building 2, FIYTA Timepiece Building, Nanhuan Avenue, Matian Sub-district, Guangming District, Shenzhen, Guangdong, 518106 P.R. China
Keywords: Comen Electrocardiograph, CMDR-2025-04122, Shenzhen Comen Medical Instruments Co., Ltd. - Floor 10, Floor 11 and Section C of Floor 12 of Building 1A 7 Floor 1 to Floor 5 of Building 2, FIYTA Timepiece Building, Nanhuan Avenue, Matian Sub-district, Guangming District, Shenzhen, Guangdong, 518106 P.R. China, Zafire Distributors, Inc., China, Philippines FDA registration

PhilippinesShenzhen Comen Medical Instruments Co., Ltd. - Floor 10, Floor 11 and Section C of Floor 12 of Building 1A 7 Floor 1 to Floor 5 of Building 2, FIYTA Timepiece Building, Nanhuan Avenue, Matian Sub-district, Guangming District, Shenzhen, Guangdong, 518106 P.R. ChinaChinaIssued March 12, 2025 – March 12, 2030

VerifiedFDA Philippines · official registry

Device information

Product Name: Comen Electrocardiograph
Registration Number: CMDR-2025-04122

Manufacturer details

Manufacturer: Shenzhen Comen Medical Instruments Co., Ltd. - Floor 10, Floor 11 and Section C of Floor 12 of Building 1A 7 Floor 1 to Floor 5 of Building 2, FIYTA Timepiece Building, Nanhuan Avenue, Matian Sub-district, Guangming District, Shenzhen, Guangdong, 518106 P.R. China
Country of Origin: China

Importer & distribution

Importer/Distributor: Zafire Distributors, Inc.

Registration dates

Issuance Date: March 12, 2025
Expiry Date: March 12, 2030

About this record

Access comprehensive regulatory information for Comen Electrocardiograph in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04122 and manufactured by Shenzhen Comen Medical Instruments Co., Ltd. - Floor 10, Floor 11 and Section C of Floor 12 of Building 1A 7 Floor 1 to Floor 5 of Building 2, FIYTA Timepiece Building, Nanhuan Avenue, Matian Sub-district, Guangming District, Shenzhen, Guangdong, 518106 P.R. China in China. The device was registered on March 12, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Zafire Distributors, 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.