Taiwan FDA registration 30daebc2f0f4880ece3eee61c4b554a7
"Le Pulse" Putt vascular occlusion catheter
TW: “樂脈”普特血管閉塞導管
Taiwan·Risk Class 2·LEMAITRE VASCULAR, INC.·Registered Oct 28, 2008 – Oct 28, 2028ActiveRegistration details
- Analysis ID
- 30daebc2f0f4880ece3eee61c4b554a7
- Customs Code
- DHA00601930701
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.1240 流量導向導管
- Import Information
- import
Dates and status
- Registration Date
- Oct 28, 2008
- Expiry Date
- Oct 28, 2028
About this record
Access comprehensive regulatory information for "Le Pulse" Putt vascular occlusion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30daebc2f0f4880ece3eee61c4b554a7 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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