DR. KELLY NEBULIZER KIT WITH MOUTHPIECE - FDA Registration MDR-09658
Access comprehensive regulatory information for DR. KELLY NEBULIZER KIT WITH MOUTHPIECE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09658 and manufactured by Ningbo Foyomed Medical Instruments Co., Ltd. in China. The device was registered on July 05, 2021.
This page provides complete registration details including manufacturer information, importer/distributor details (Medical Center 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.
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China
MDR-09658
DR. KELLY NEBULIZER KIT WITH MOUTHPIECE
Registered medical device in Philippines
Device Information
Product Name
DR. KELLY NEBULIZER KIT WITH MOUTHPIECE
Registration Number
MDR-09658
Manufacturer Details
Manufacturer
Ningbo Foyomed Medical Instruments Co., Ltd.Country of Origin
China
Importer & Distribution
Importer/Distributor
Medical Center Trading CorporationRegistration Dates
Issuance Date
July 05, 2021
Expiry Date
May 13, 2026

