Taiwan FDA registration 1b729d68c71c7b00b84cc9eec413d42e
"Hekoma" upper limb rehabilitation device (unsterilized)
TW: “賀可瑪”上肢復健裝置(未滅菌)
Taiwan·Risk Class 1·HOCOMA AT·Registered May 12, 2008 – May 12, 2013CancelledRegistration details
- Analysis ID
- 1b729d68c71c7b00b84cc9eec413d42e
- Customs Code
- DHA04400674304
Company information
- Manufacturer
- HOCOMA AT
- Manufacturer Country
- Switzerland
- Authorized Representative
- AMPLE MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
- Import Information
- import
Dates and status
- Registration Date
- May 12, 2008
- Expiry Date
- May 12, 2013
- Cancellation Date
- Mar 14, 2012
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Hekoma" upper limb rehabilitation device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1b729d68c71c7b00b84cc9eec413d42e and manufactured by HOCOMA AT. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..
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