Taiwan FDA registration a364b4e20c45f19eb62353e75114358f
"Rehabilitation Home" mechanical wheelchair (unsterilized)
TW: "康復之家" 機械式輪椅 (未滅菌)
Taiwan·Risk Class 1·MIKI (SHANGHAI) CO., LTD.·Registered Aug 05, 2013 – Aug 05, 2018CancelledRegistration details
- Analysis ID
- a364b4e20c45f19eb62353e75114358f
- Customs Code
- DHA09600194105
Company information
- Manufacturer
- MIKI (SHANGHAI) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Rehabilitation Home Medical Equipment Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Mechanical Wheelchair (O.3850)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3850 Mechanical wheelchairs
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 05, 2013
- Expiry Date
- Aug 05, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Rehabilitation Home" mechanical wheelchair (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a364b4e20c45f19eb62353e75114358f and manufactured by MIKI (SHANGHAI) CO., LTD.. The authorized representative in Taiwan is Rehabilitation Home Medical Equipment Co., Ltd.
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