Taiwan FDA registration 974abd0e0ec17b2b1320db42c83e54d4
"Kyobeshi" manual hospital bed (unsterilized)
TW: "京倍思" 手動病床 (未滅菌)
Taiwan·Risk Class 1·JIN PRAISE MEDICAL TREATMENT INSTRUMENTS CO., LTD.·Registered Dec 15, 2015 – Dec 15, 2020CancelledRegistration details
- Analysis ID
- 974abd0e0ec17b2b1320db42c83e54d4
- Customs Code
- DHA09600259109
Company information
- Manufacturer Country
- China
- Authorized Representative
- HOSPITAL KEEPER TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Manual Adjustable Hospital Bed (J.5120)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5120 手動可調整式病床
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Dec 15, 2015
- Expiry Date
- Dec 15, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kyobeshi" manual hospital bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 974abd0e0ec17b2b1320db42c83e54d4 and manufactured by JIN PRAISE MEDICAL TREATMENT INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is HOSPITAL KEEPER TECHNOLOGY CO., LTD..
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