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Rusch Guedel Airway - FDA Registration DVR-7489

Access comprehensive regulatory information for Rusch Guedel Airway in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-7489 and manufactured by Teleflex Medical- -IDA Business and Technology Park, Dublin Road, Athlone, Co.,Westmeath, Ireland Mfd by: Foremount Enterprise Co. Ltd.-No. 17, Alley 15, Lane 5, Shenan Street, Shengang Dist., Taichuing City 42944, Taiwan in Taiwan. The device was registered on February 13, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (East Lane 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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Taiwan
DVR-7489
Rusch Guedel Airway
Registered medical device in Philippines
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Importer & Distribution
Importer/Distributor
East Lane Corporation
Registration Dates
Issuance Date
February 13, 2025
Expiry Date
September 10, 2029