Taiwan FDA registration 4a4f3cec1abf0f17e1f1dfaa76ba16e6
"Xinli" high-pressure contrast injection extension tube
TW: “昕力”高壓造影注射延長管
Taiwan·Risk Class 2·SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.·Registered Feb 14, 2017 – Feb 14, 2027ActiveRegistration details
- Analysis ID
- 4a4f3cec1abf0f17e1f1dfaa76ba16e6
- Customs Code
- DHA09200081400
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
- Feb 14, 2017
- Expiry Date
- Feb 14, 2027
About this record
Access comprehensive regulatory information for "Xinli" high-pressure contrast injection extension tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4a4f3cec1abf0f17e1f1dfaa76ba16e6 and manufactured by SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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