Taiwan FDA registration f6aad0d7a7b9454e7ecfc420269e6fdc
"Kemei" Reverse Fox (with needle \ without needle)
TW: "科美" 逆福仕 (附針＼不附針)
Taiwan·Q-MED AB·Registered Jul 21, 2003 – Jul 21, 2013CancelledRegistration details
- Analysis ID
- f6aad0d7a7b9454e7ecfc420269e6fdc
- Customs Code
- DHA00601034602
Company information
- Manufacturer
- Q-MED AB
- Manufacturer Country
- Sweden
- Authorized Representative
- Taiwan Meiqiang Co., Ltd
Product details
- Intended Use
- 1. Stress-induced urinary incontinence caused by urethral sphincter insufficiency. 2. Vesicoureteral reflux.
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Jul 21, 2003
- Expiry Date
- Jul 21, 2013
- Cancellation Date
- Apr 23, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kemei" Reverse Fox (with needle \ without needle) in Taiwan's medical device market through Pure Global AI's free database. is registered under number f6aad0d7a7b9454e7ecfc420269e6fdc and manufactured by Q-MED AB. The authorized representative in Taiwan is Taiwan Meiqiang Co., Ltd.
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