Taiwan FDA registration 8bc4aa028b997490ac07ddb12347135e
"Le Pulse" expandable valve knife
TW: “樂脈”可擴張式瓣膜刀
Taiwan·Risk Class 2·LEMAITRE VASCULAR, INC.·Registered Dec 21, 2009 – Dec 21, 2019CancelledRegistration details
- Analysis ID
- 8bc4aa028b997490ac07ddb12347135e
- Customs Code
- DHA00602050502
Company information
- Manufacturer
- LEMAITRE VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HSIN TUNG MEDICAL 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.4885 靜脈血管剝離器
- Import Information
- import
Dates and status
- Registration Date
- Dec 21, 2009
- Expiry Date
- Dec 21, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Le Pulse" expandable valve knife in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8bc4aa028b997490ac07ddb12347135e and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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