Taiwan FDA registration 9b82e36cf09325006dc6cf9efad89cae
"Xiangyuan" intranasal fixation splint (unsterilized)
TW: “翔源”鼻腔內固定夾板 (未滅菌)
Taiwan·Risk Class 1·MAXIGEN BIOTECH INC.·Registered Aug 05, 2013 – Aug 05, 2018CancelledRegistration details
- Analysis ID
- 9b82e36cf09325006dc6cf9efad89cae
Company information
- Manufacturer
- MAXIGEN BIOTECH INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MEDFRONT MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of "Intranasal Splint (G.4780)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4780 Nasal fixations
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Aug 05, 2013
- Expiry Date
- Aug 05, 2018
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Xiangyuan" intranasal fixation splint (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9b82e36cf09325006dc6cf9efad89cae and manufactured by MAXIGEN BIOTECH INC.. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.
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