Taiwan FDA registration 5bdf91cfb884bba09e0d1df6c1626c59
"Kangqier" Shi Shi Mark capsules
TW: “康賜爾”西施馬克膠囊
Taiwan·Risk Class 3·KONSYL PHARMACEUTICALS, INC.·Registered Apr 12, 2007 – Apr 12, 2012CancelledRegistration details
- Analysis ID
- 5bdf91cfb884bba09e0d1df6c1626c59
- Customs Code
- DHA00601825500
Company information
- Manufacturer
- KONSYL PHARMACEUTICALS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WELL SHIP INDUSTRIAL CO., LTD.
Product details
- Intended Use
- For details, please refer to the approved version of Chinese copy.
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Apr 12, 2007
- Expiry Date
- Apr 12, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kangqier" Shi Shi Mark capsules in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5bdf91cfb884bba09e0d1df6c1626c59 and manufactured by KONSYL PHARMACEUTICALS, INC.. The authorized representative in Taiwan is WELL SHIP INDUSTRIAL CO., LTD..
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