Taiwan FDA registration 6f7ccfe61d0c2cd2a8837d54ac7aeaeb
"Xinli" disposable connector
TW: “昕力”一次性使用連通器
Taiwan·Risk Class 2·SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.·Registered Mar 27, 2017 – Mar 27, 2027ActiveRegistration details
- Analysis ID
- 6f7ccfe61d0c2cd2a8837d54ac7aeaeb
- Customs Code
- DHA09200081900
Company information
- Manufacturer
- SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- CATHERINE CONSULTANTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1650 血管攝影注射器和注射筒
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 27, 2017
- Expiry Date
- Mar 27, 2027
About this record
Access comprehensive regulatory information for "Xinli" disposable connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6f7ccfe61d0c2cd2a8837d54ac7aeaeb and manufactured by SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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