Philippines FDA registration CMDR-2025-05040

Ormed Humidifier Bubble

Name: Ormed Humidifier Bubble — Philippines FDA registration CMDR-2025-05040
Creator: Ningbo Foyomed Medical Instruments Co., Ltd. - 9F, Ningshing Building, No.666 Jiang Nan Road, Ningbo, China
Keywords: Ormed Humidifier Bubble, CMDR-2025-05040, Ningbo Foyomed Medical Instruments Co., Ltd. - 9F, Ningshing Building, No.666 Jiang Nan Road, Ningbo, China, Impexcos Co., China, Philippines FDA registration

PhilippinesNingbo Foyomed Medical Instruments Co., Ltd. - 9F, Ningshing Building, No.666 Jiang Nan Road, Ningbo, ChinaChinaIssued July 11, 2025 – July 11, 2030

VerifiedFDA Philippines · official registry

Device information

Product Name: Ormed Humidifier Bubble
Registration Number: CMDR-2025-05040

Manufacturer details

Manufacturer: Ningbo Foyomed Medical Instruments Co., Ltd. - 9F, Ningshing Building, No.666 Jiang Nan Road, Ningbo, China
Country of Origin: China

Importer & distribution

Importer/Distributor: Impexcos Co.

Registration dates

Issuance Date: July 11, 2025
Expiry Date: July 11, 2030

About this record

Access comprehensive regulatory information for Ormed Humidifier Bubble in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-05040 and manufactured by Ningbo Foyomed Medical Instruments Co., Ltd. - 9F, Ningshing Building, No.666 Jiang Nan Road, Ningbo, China in China. The device was registered on July 11, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Impexcos Co.), 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.