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"DVI" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile) - Taiwan Registration 80013cfae8781615e9755b7bdb6d2345

Access comprehensive regulatory information for "DVI" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 80013cfae8781615e9755b7bdb6d2345 and manufactured by DESIGNS FOR VISION, INC.. The authorized representative in Taiwan is Liren Equipment Factory Co., Ltd.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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80013cfae8781615e9755b7bdb6d2345
Registration Details
Taiwan FDA Registration: 80013cfae8781615e9755b7bdb6d2345
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Device Details

"DVI" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile)
TW: "็ฌฌ็ถญๆ„›" ่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

80013cfae8781615e9755b7bdb6d2345

Ministry of Health Medical Device Import No. 016834

DHA09401683406

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".

G ENT device

G4350 ENT fiber optic light source and vehicle

Imported from abroad

Dates and Status

Jul 28, 2016

Jul 28, 2021