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Simplex® Endotracheal Tube Uncuffed (Sterile) - FDA Registration DVR-5777

Access comprehensive regulatory information for Simplex® Endotracheal Tube Uncuffed (Sterile) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-5777 and manufactured by Ningbo Greatcare Trading Co., Ltd. - Unit 93, Building 12, No. 818, Qiming Road, Yinzhou, Ningbo 315105, Zhejiang, China Mfd by: Well Lead Medical Co., Ltd. - C-4 Jinhu Industrial Estate, Hualong 511434 Panyu, Guangzhou, China in China. The device was registered on November 08, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Panamed Philippines, 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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DVR-5777
Simplex® Endotracheal Tube Uncuffed (Sterile)
Registered medical device in Philippines
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Device Information
Product Name
Simplex® Endotracheal Tube Uncuffed (Sterile)
Registration Number
DVR-5777
Importer & Distribution
Importer/Distributor
Panamed Philippines, Inc.
Registration Dates
Issuance Date
November 08, 2024
Expiry Date
January 27, 2029