Taiwan FDA registration 944103344d5b726574415dced6a0e1ff
"Tister" plaster removal device (unsterilized)
TW: “蒂氏特”石膏拆除器械 (未滅菌)
Taiwan·Risk Class 1·DE SOUTTER MEDICAL LIMITED·Registered Jun 18, 2012 – Jun 18, 2022CancelledRegistration details
- Analysis ID
- 944103344d5b726574415dced6a0e1ff
- Customs Code
- DHA04401183901
Company information
- Manufacturer
- DE SOUTTER MEDICAL LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Gypsum Removal Devices (N.5960)".
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.5960 石膏拆除器械
- Import Information
- import
Dates and status
- Registration Date
- Jun 18, 2012
- Expiry Date
- Jun 18, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Tister" plaster removal device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 944103344d5b726574415dced6a0e1ff and manufactured by DE SOUTTER MEDICAL LIMITED. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..
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