Taiwan FDA registration 486da09254fbc2245781a58dfa0cd341
"Shisei" nonwoven gauze mat (unsterilized)
TW: “資生” 不織布紗布墊 (未滅菌)
Taiwan·Risk Class 1·HUBEI QIANJIANG KINGPHAR MEDICAL MATERIAL CO., LTD·Registered May 04, 2020 – May 04, 2025ExpiredRegistration details
- Analysis ID
- 486da09254fbc2245781a58dfa0cd341
- Customs Code
- DHA09600416005
Company information
- Manufacturer Country
- China
- Authorized Representative
- SHI SEI INTERNATIONAL LIMITED
Product details
- Intended Use
- Limited to the first level of classification and grading management of medical devices "external use of non-absorbent gauze or sponge balls (I.4014)" identification range.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4014 Non-absorbent cloth or sea balls are used externally
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- May 04, 2020
- Expiry Date
- May 04, 2025
About this record
Access comprehensive regulatory information for "Shisei" nonwoven gauze mat (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 486da09254fbc2245781a58dfa0cd341 and manufactured by HUBEI QIANJIANG KINGPHAR MEDICAL MATERIAL CO., LTD. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.
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