Taiwan FDA registration 98be246c7abaf67d7182b6619b8fa012
"Nasal comfort" physiological seawater neti wash (sterilization)
TW: "鼻舒適" 生理海水洗鼻器 (滅菌)
Taiwan·Risk Class 1·URGO LABORATORIES·Registered Jan 29, 2015 – Jan 29, 2020CancelledRegistration details
- Analysis ID
- 98be246c7abaf67d7182b6619b8fa012
- Customs Code
- DHA09401488704
Company information
- Manufacturer
- URGO LABORATORIES
- Manufacturer Country
- France
- Authorized Representative
- ZUELLIG PHARMA, INC.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Dispensing Devices (G.5220)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 29, 2015
- Expiry Date
- Jan 29, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nasal comfort" physiological seawater neti wash (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98be246c7abaf67d7182b6619b8fa012 and manufactured by URGO LABORATORIES. The authorized representative in Taiwan is ZUELLIG PHARMA, INC..
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