Taiwan FDA registration 19fd5c982133531923bedb6bbb852b06
"Swanmotown" scalpel blade (sterilized)
TW: "史旺摩敦" 手術刀片 (滅菌)
Taiwan·Risk Class 1·SWANN-MORTON LIMITED·Registered Mar 15, 2021 – Mar 15, 2026ExpiredRegistration details
- Analysis ID
- 19fd5c982133531923bedb6bbb852b06
- Customs Code
- DHA09402238502
Company information
- Manufacturer
- SWANN-MORTON LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- THREE A CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 15, 2021
- Expiry Date
- Mar 15, 2026
About this record
Access comprehensive regulatory information for "Swanmotown" scalpel blade (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 19fd5c982133531923bedb6bbb852b06 and manufactured by SWANN-MORTON LIMITED. The authorized representative in Taiwan is THREE A CO., LTD..
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