Taiwan FDA registration 4dda184f73f887604a5c5d4a51fb3614
"Xinli" single-use Y-connector kit
TW: “昕力”一次性使用Y型連接器套件
Taiwan·Risk Class 2·Sunny Medical Device (Shenzhen) Co., Ltd.·Registered Jan 18, 2019 – Jan 18, 2029ActiveRegistration details
- Analysis ID
- 4dda184f73f887604a5c5d4a51fb3614
- Customs Code
- DHA09200097702
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.4290 Arterial vascular bypass surgery with contact pistons, multi-pipe connections or attachments
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jan 18, 2019
- Expiry Date
- Jan 18, 2029
About this record
Access comprehensive regulatory information for "Xinli" single-use Y-connector kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4dda184f73f887604a5c5d4a51fb3614 and manufactured by Sunny Medical Device (Shenzhen) Co., Ltd.. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
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