Taiwan FDA registration 2e2a8679304ba7ec8bcef19bec75435f
"Le Pulse" arterial thrombus clearance catheter
TW: “樂脈”動脈血栓清除導管
Taiwan·Risk Class 2·LEMAITRE VASCULAR, INC.·Registered Apr 24, 2008 – Apr 24, 2028ActiveRegistration details
- Analysis ID
- 2e2a8679304ba7ec8bcef19bec75435f
- Customs Code
- DHA00601881502
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.5150 血栓切除術導管
- Import Information
- import
Dates and status
- Registration Date
- Apr 24, 2008
- Expiry Date
- Apr 24, 2028
About this record
Access comprehensive regulatory information for "Le Pulse" arterial thrombus clearance catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2e2a8679304ba7ec8bcef19bec75435f and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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