Taiwan FDA registration 9483375422be272baae5047003b60849
Reanda Non-AC Electric Patient Lift (Unsterilized)
TW: "利安達" 非交流電力式病患升降機 (未滅菌)
Taiwan·Risk Class 1·SUZHOU IRELAND MEDICAL EQUIPMENT CO., LTD·Registered Apr 27, 2021 – Apr 27, 2026CancelledRegistration details
- Analysis ID
- 9483375422be272baae5047003b60849
- Customs Code
- DHA09600451006
Company information
- Manufacturer
- SUZHOU IRELAND MEDICAL EQUIPMENT CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- PROMEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5510 Non-AC electric patient lifts
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 27, 2021
- Expiry Date
- Apr 27, 2026
- Cancellation Date
- Sep 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Reanda Non-AC Electric Patient Lift (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9483375422be272baae5047003b60849 and manufactured by SUZHOU IRELAND MEDICAL EQUIPMENT CO., LTD. The authorized representative in Taiwan is PROMEDICAL CO., LTD..
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