Taiwan FDA registration f7378fc2e059c758814e221a49e5b082
"Bidi I" isokinetic muscle strength test evaluation system
TW: “必帝一”等速肌力試驗評估系統
Taiwan·Risk Class 1·BTE TECHNOLOGIES, INC.·Registered Aug 03, 2006 – Aug 03, 2011CancelledRegistration details
- Analysis ID
- f7378fc2e059c758814e221a49e5b082
- Customs Code
- DHA04400501505
Company information
- Manufacturer
- BTE TECHNOLOGIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WHOLE WELL CO., LTD.
Product details
- Intended Use
- It is limited to the first level of identification scope of the "Isokinetic Muscle Strength Test Evaluation System (O.1925)" of the Administrative Measures for Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.1925 等速肌力試驗評估系統
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Aug 03, 2006
- Expiry Date
- Aug 03, 2011
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bidi I" isokinetic muscle strength test evaluation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7378fc2e059c758814e221a49e5b082 and manufactured by BTE TECHNOLOGIES, INC.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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