Philippines FDA registration CMDR-2025-04828

Edan Pulse Oximeter

Philippines·Edan Instruments, Inc. - #15 Jinhui ROad, Jinsha Community, Kengzi Sub-District, Pingshan DIstrict, 518122 Shenzhen, China·China·Issued June 05, 2025 – June 03, 2030

Device information

Product Name: Edan Pulse Oximeter
Registration Number: CMDR-2025-04828

Manufacturer details

Manufacturer: Edan Instruments, Inc. - #15 Jinhui ROad, Jinsha Community, Kengzi Sub-District, Pingshan DIstrict, 518122 Shenzhen, China
Country of Origin: China

Importer & distribution

Importer/Distributor: Biosite Medical Instruments

Registration dates

Issuance Date: June 05, 2025
Expiry Date: June 03, 2030

About this record

Access comprehensive regulatory information for Edan Pulse Oximeter in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04828 and manufactured by Edan Instruments, Inc. - #15 Jinhui ROad, Jinsha Community, Kengzi Sub-District, Pingshan DIstrict, 518122 Shenzhen, China in China. The device was registered on June 05, 2025.

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