Taiwan FDA registration 9bc104759fa8cef0c7d9ad3201b00a13
"Lepu" amber percutaneous puncture coronary balloon catheter
TW: “樂普”琥珀經皮穿刺冠狀動脈球囊導管
Taiwan·Risk Class 3·Lepu Medical Technology (Beijing) Co., Ltd.·Registered Apr 25, 2014 – Apr 25, 2019CancelledRegistration details
- Analysis ID
- 9bc104759fa8cef0c7d9ad3201b00a13
- Customs Code
- DHA09200058702
Company information
- Manufacturer
- Lepu Medical Technology (Beijing) Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- SUNNY HEART SCIENTIFIC 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.0005.
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Apr 25, 2014
- Expiry Date
- Apr 25, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Lepu" amber percutaneous puncture coronary balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9bc104759fa8cef0c7d9ad3201b00a13 and manufactured by Lepu Medical Technology (Beijing) Co., Ltd.. The authorized representative in Taiwan is SUNNY HEART SCIENTIFIC CO., LTD..
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