Taiwan FDA registration 1aeacaf94832fc061f8d3d8412d88d3c
"Le Pulse" Neotel thrombus removal catheter
TW: “樂脈”新特爾血栓清除導管
Taiwan·Risk Class 2·LEMAITRE VASCULAR, INC.·Registered May 18, 2011 – May 18, 2026ExpiredRegistration details
- Analysis ID
- 1aeacaf94832fc061f8d3d8412d88d3c
- Customs Code
- DHA00602231609
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.5150 血栓切除術導管
- Import Information
- import
Dates and status
- Registration Date
- May 18, 2011
- Expiry Date
- May 18, 2026
About this record
Access comprehensive regulatory information for "Le Pulse" Neotel thrombus removal catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1aeacaf94832fc061f8d3d8412d88d3c and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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