Taiwan FDA registration 81322e7316846942b9bc17d3338c110f
"Le Pulse" Putt aorta blocks the catheter
TW: “樂脈”普特主動脈阻斷導管
Taiwan·Risk Class 2·LEMAITRE VASCULAR, INC.·Registered Jun 01, 2009 – Jun 01, 2029ActiveRegistration details
- Analysis ID
- 81322e7316846942b9bc17d3338c110f
- Customs Code
- DHA00601988206
Company information
- Manufacturer
- LEMAITRE VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FRONTIER BIO-MEDICAL INC.
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.4450 Vascular clips
- Import Information
- import
Dates and status
- Registration Date
- Jun 01, 2009
- Expiry Date
- Jun 01, 2029
About this record
Access comprehensive regulatory information for "Le Pulse" Putt aorta blocks the catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 81322e7316846942b9bc17d3338c110f and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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