Taiwan FDA registration ef657c91ef6233593423e4cf2c674e64
"Kangenfei" powered treatment unit (non-sterilized)
TW: "康恩菲" 動力式治療檯 (未滅菌)
Taiwan·Risk Class 1·HUANGSHAN JINFU MEDICAL EQUIPMENT CO., LTD.·Registered Oct 21, 2024 – Oct 21, 2029ActiveRegistration details
- Analysis ID
- ef657c91ef6233593423e4cf2c674e64
- Customs Code
- DHA09600501004
Company information
- Manufacturer
- HUANGSHAN JINFU MEDICAL EQUIPMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- RUI-HUNG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the "Power Treatment Table (O.3760)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3760 Powered therapy cage
- Import Information
- QMS/QSD;; Input;; Chinese goods
Dates and status
- Registration Date
- Oct 21, 2024
- Expiry Date
- Oct 21, 2029
About this record
Access comprehensive regulatory information for "Kangenfei" powered treatment unit (non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef657c91ef6233593423e4cf2c674e64 and manufactured by HUANGSHAN JINFU MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is RUI-HUNG INSTRUMENTS CO., LTD..
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