Pure Global

"Daiichi" Ear, nose, and throat examination and treatment unit (Non-Sterile) - Taiwan Registration 6cce27d79de3a5366d46dcb64b872cc2

Access comprehensive regulatory information for "Daiichi" Ear, nose, and throat examination and treatment unit (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 6cce27d79de3a5366d46dcb64b872cc2 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
6cce27d79de3a5366d46dcb64b872cc2
Registration Details
Taiwan FDA Registration: 6cce27d79de3a5366d46dcb64b872cc2
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Daiichi" Ear, nose, and throat examination and treatment unit (Non-Sterile)
TW: "ๅคงๅฃนๅ™จ" ่€ณ้ผปๅ–‰ๆชขๆŸฅๅŠๆฒป็™‚ๆชฏ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6cce27d79de3a5366d46dcb64b872cc2

Ministry of Health Medical Device Import No. 013277

DHA09401327701

Company Information

Japan

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Examination and Treatment Unit (G.5300)".

G ENT device

G5300 ENT Examination and Treatment Unit

Imported from abroad

Dates and Status

Aug 05, 2013

Aug 05, 2023