Taiwan FDA registration 21b8d7f9d24bcc98b7468253e739e75d
"Lepu" Anxing single-use angiography catheter
TW: “樂普”安蕎星一次性使用血管造影導管
Taiwan·Risk Class 2·Lepu Medical Technology (Beijing) Co., Ltd.·Registered Jun 17, 2015 – Jun 17, 2020CancelledRegistration details
- Analysis ID
- 21b8d7f9d24bcc98b7468253e739e75d
- Customs Code
- DHA09200065901
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.1200 診斷用血管內導管
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jun 17, 2015
- Expiry Date
- Jun 17, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Lepu" Anxing single-use angiography catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21b8d7f9d24bcc98b7468253e739e75d and manufactured by Lepu Medical Technology (Beijing) Co., Ltd.. The authorized representative in Taiwan is SUNNY HEART SCIENTIFIC CO., LTD..
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