Taiwan FDA registration 3ef191eb72c1819cd97286d6fded850c
"Nasaleze" Nose and Throat Drug Administration Device (Non-Sterile)
TW: "諾舒宜"鼻喉佈施藥裝置(未滅菌)
Taiwan·Risk Class 1·MD·NASALEZE LTD.·Registered Aug 04, 2014 – Aug 04, 2019CancelledRegistration details
- Analysis ID
- 3ef191eb72c1819cd97286d6fded850c
- License Form
- Ministry of Health Medical Device Import No. 014402
- Customs Code
- DHA09401440206
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 device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 04, 2014
- Expiry Date
- Aug 04, 2019
- Cancellation Date
- Aug 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
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..
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