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Reditube™ Tracheal Tube Oral/Nasal with Preloaded Stylet - Cuffed - FDA Registration DVR-8283

Access comprehensive regulatory information for Reditube™ Tracheal Tube Oral/Nasal with Preloaded Stylet - Cuffed in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-8283 and manufactured by Vyaire Medical Inc. 26125 N. Riverwoods Blvd. Mettawa, IL 60045, USA Mfd By: Well Lead Medical Co., Ltd. - C-4, Jinhu Industrial Estate, Hualong, 511434 Panyu, Guanzhou, China in USA. The device was registered on February 14, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Healthsolutions Enterprises 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-8283
Reditube™ Tracheal Tube Oral/Nasal with Preloaded Stylet - Cuffed
Registered medical device in Philippines
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Device Information
Product Name
Reditube™ Tracheal Tube Oral/Nasal with Preloaded Stylet - Cuffed
Registration Number
DVR-8283
Importer & Distribution
Registration Dates
Issuance Date
February 14, 2024
Expiry Date
April 13, 2026