Taiwan FDA registration 24452d8bcba47c50acdd4d213ed7c799
“Nasaleze” Allergy (Non-Sterile)
TW: “諾舒宜”安敏噴劑(未滅菌)
Taiwan·Risk Class 2·MD·NASALEZE LTD.·Registered Oct 26, 2016 – Oct 26, 2021CancelledRegistration details
- Analysis ID
- 24452d8bcba47c50acdd4d213ed7c799
- License Form
- Ministry of Health Medical Device Import No. 028803
- Customs Code
- DHA05602880304
Company information
- Manufacturer
- NASALEZE LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- MEDBEST ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G5220 ENT dosing devices and substances used in conjunction with them
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 26, 2016
- Expiry Date
- Oct 26, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
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..
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