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Endosoft Endotracheal Tubes Cuffed, Oral/Nasal - FDA Registration MDR-10038

Access comprehensive regulatory information for Endosoft Endotracheal Tubes Cuffed, Oral/Nasal in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10038 and manufactured by Zhanjiang Star Enterprise Co., Ltd. No. 1, West Jinhua Road Mazhang District 524094 Zhanjiang People's Republic of China in China. The device was registered on May 28, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Alvez Commercial, 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.

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China
MDR-10038
Endosoft Endotracheal Tubes Cuffed, Oral/Nasal
Registered medical device in Philippines
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Device Information
Product Name
Endosoft Endotracheal Tubes Cuffed, Oral/Nasal
Registration Number
MDR-10038
Importer & Distribution
Importer/Distributor
Alvez Commercial, Inc.
Registration Dates
Issuance Date
May 28, 2024
Expiry Date
July 23, 2026