Taiwan FDA registration b0fa85e84b6f16384d6bf4eea57d380f
"Xinli" guide wire
TW: “昕力”導引導線
Taiwan·Risk Class 2·Sunny Medical Device (Shenzhen) Co., Ltd.·Registered Jan 16, 2019 – Jan 16, 2029ActiveRegistration details
- Analysis ID
- b0fa85e84b6f16384d6bf4eea57d380f
- Customs Code
- DHA09200097600
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.1330 Catheter Guide Wires
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 16, 2019
- Expiry Date
- Jan 16, 2029
About this record
Access comprehensive regulatory information for "Xinli" guide wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0fa85e84b6f16384d6bf4eea57d380f and manufactured by Sunny Medical Device (Shenzhen) Co., Ltd.. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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