Taiwan FDA registration 6d972c40d0c9b90e3102751400977246
"Distin" plaster removal device (unsterilized)
TW: "狄司特" 石膏拆除器械(未滅菌)
Taiwan·Risk Class 1·DE SOUTTER MEDICAL LTD·Registered Jun 28, 2023 – Jun 28, 2028ActiveRegistration details
- Analysis ID
- 6d972c40d0c9b90e3102751400977246
- Customs Code
- DHA09402316404
Company information
- Manufacturer
- DE SOUTTER MEDICAL LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- CHAWEI CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures for medical equipment, gypsum removal equipment (N.5960) first grade identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.5960 石膏拆除器械
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jun 28, 2023
- Expiry Date
- Jun 28, 2028
About this record
Access comprehensive regulatory information for "Distin" 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 6d972c40d0c9b90e3102751400977246 and manufactured by DE SOUTTER MEDICAL LTD. The authorized representative in Taiwan is CHAWEI CO., LTD..
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