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Endotracheal Tube Pedia (Uncuffed) Sterile - FDA Registration DVR-5846

Access comprehensive regulatory information for Endotracheal Tube Pedia (Uncuffed) Sterile in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-5846 and manufactured by Kenxin International Company Ltd. Rooftop, 19 Sun Hong Street, Sheung Shui, New Territories, Hongkong Mfd. By: Kenxin International Company Ltd. - Rm. 714 Huagang Office Building no. 140 Zhongshandadao, Guangzhou China in Hongkong. The device was registered on October 26, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Indoplas 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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Hongkong
DVR-5846
Endotracheal Tube Pedia (Uncuffed) Sterile
Registered medical device in Philippines
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Device Information
Product Name
Endotracheal Tube Pedia (Uncuffed) Sterile
Registration Number
DVR-5846
Importer & Distribution
Importer/Distributor
Indoplas Philippines Inc.
Registration Dates
Issuance Date
October 26, 2023
Expiry Date
March 28, 2028