Taiwan FDA registration bbca1f4b5c7a83995b1812f3cf5fc9af
YIKA patient transfer device (Non-sterile)
TW: 宜康 病患移位裝置 (未滅菌)
Taiwan·Risk Class 1·MD·YIKA MEDICAL CO., LTD.·Registered Apr 08, 2022 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- bbca1f4b5c7a83995b1812f3cf5fc9af
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. a00052
Company information
- Manufacturer
- YIKA MEDICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YIKA MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Patient Transport Device (J.6785)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6785 Manual Patient Conveyor
Dates and status
- Registration Date
- Apr 08, 2022
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for YIKA patient transfer device (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bbca1f4b5c7a83995b1812f3cf5fc9af and manufactured by YIKA MEDICAL CO., LTD.. The authorized representative in Taiwan is YIKA MEDICAL CO., LTD..
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