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"Nasaleze" Nose and Throat Drug Administration Device (Non-Sterile) - Taiwan Registration 3ef191eb72c1819cd97286d6fded850c

Access comprehensive regulatory information for "Nasaleze" Nose and Throat Drug Administration Device (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 3ef191eb72c1819cd97286d6fded850c and manufactured by NASALEZE LTD.. The authorized representative in Taiwan is MEDBEST ENTERPRISE 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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3ef191eb72c1819cd97286d6fded850c
Registration Details
Taiwan FDA Registration: 3ef191eb72c1819cd97286d6fded850c
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Device Details

"Nasaleze" Nose and Throat Drug Administration Device (Non-Sterile)
TW: "่ซพ่ˆ’ๅฎœ"้ผปๅ–‰ไฝˆๆ–ฝ่—ฅ่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

3ef191eb72c1819cd97286d6fded850c

Ministry of Health Medical Device Import No. 014402

DHA09401440206

Company Information

United Kingdom

Product Details

G ENT device

G5220 ENT dosing device

Imported from abroad

Dates and Status

Aug 04, 2014

Aug 04, 2019

Aug 13, 2019

Cancellation Information

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