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"Daiichi" Ear, nose, and throat fiberoptic light source and carrier (Non-Sterile) - Taiwan Registration 1623b0396a72bc71ea8bd0fd4f247392

Access comprehensive regulatory information for "Daiichi" 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 1623b0396a72bc71ea8bd0fd4f247392 and manufactured by DAIICHI MEDICAL CO., LTD.. The authorized representative in Taiwan is GIA HO INSTRUMENTS 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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1623b0396a72bc71ea8bd0fd4f247392
Registration Details
Taiwan FDA Registration: 1623b0396a72bc71ea8bd0fd4f247392
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Device Details

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

Registration Details

1623b0396a72bc71ea8bd0fd4f247392

Ministry of Health Medical Device Import No. 013276

DHA09401327609

Company Information

Japan

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

Aug 05, 2013

Aug 05, 2028