Taiwan FDA registration a970867bebc678ea458822a4bb96e353
"HOKOMA" isokinetic strength test evaluation system (unsterilized)
TW: “賀可瑪” 等速肌力試驗評估系統(未滅菌)
Taiwan·Risk Class 1·HOCOMA AT·Registered Jan 31, 2012 – Jan 31, 2017CancelledRegistration details
- Analysis ID
- a970867bebc678ea458822a4bb96e353
- Customs Code
- DHA04401132608
Company information
- Manufacturer
- HOCOMA AT
- Manufacturer Country
- Switzerland
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Isokinetic Muscle Strength Test Evaluation System (O.1925)".
- 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
- Jan 31, 2012
- Expiry Date
- Jan 31, 2017
- Cancellation Date
- Nov 26, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "HOKOMA" isokinetic strength test evaluation system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a970867bebc678ea458822a4bb96e353 and manufactured by HOCOMA AT. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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