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“Nasaleze” Allergy (Non-Sterile) - Taiwan Registration 24452d8bcba47c50acdd4d213ed7c799

Access comprehensive regulatory information for “Nasaleze” Allergy (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 24452d8bcba47c50acdd4d213ed7c799 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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24452d8bcba47c50acdd4d213ed7c799
Registration Details
Taiwan FDA Registration: 24452d8bcba47c50acdd4d213ed7c799
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Device Details

“Nasaleze” Allergy (Non-Sterile)
TW: “諾舒宜”安敏噴劑(未滅菌)
Risk Class 2
MD
Cancelled

Registration Details

24452d8bcba47c50acdd4d213ed7c799

Ministry of Health Medical Device Import No. 028803

DHA05602880304

Company Information

United Kingdom

Product Details

G ENT device

G5220 ENT dosing devices and substances used in conjunction with them

Imported from abroad

Dates and Status

Oct 26, 2016

Oct 26, 2021

Sep 08, 2023

Cancellation Information

Logged out

未展延而逾期者