Taiwan FDA registration 35d303b79cc21a3b40347e7bc64d690a
"Väcker" manual patient transport device (unsterilized)
TW: "偉克"手動病患輸送裝置(未滅菌)
Taiwan·Risk Class 1·XIAMEN TAIFU MEDICAL CO., LTD.·Registered Feb 01, 2013 – Feb 01, 2018CancelledRegistration details
- Analysis ID
- 35d303b79cc21a3b40347e7bc64d690a
- Customs Code
- DHA04600183309
Company information
- Manufacturer
- XIAMEN TAIFU MEDICAL CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- SHIN-I MEDICAL MANUFACTURING CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6785 Manual Patient Conveying Device
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Feb 01, 2013
- Expiry Date
- Feb 01, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Väcker" manual patient transport 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 35d303b79cc21a3b40347e7bc64d690a and manufactured by XIAMEN TAIFU MEDICAL CO., LTD.. The authorized representative in Taiwan is SHIN-I MEDICAL MANUFACTURING CO., LTD..
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