Taiwan FDA registration 58e3524ca029b0337f32b2f3773db9be
"Le Pulse" remote perfusion catheter
TW: “樂脈”遠端灌流導管
Taiwan·Risk Class 2·LEMAITRE VASCULAR, INC.·Registered Apr 15, 2008 – Apr 15, 2028ActiveRegistration details
- Analysis ID
- 58e3524ca029b0337f32b2f3773db9be
- Customs Code
- DHA00601879700
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.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
- Import Information
- import
Dates and status
- Registration Date
- Apr 15, 2008
- Expiry Date
- Apr 15, 2028
About this record
Access comprehensive regulatory information for "Le Pulse" remote perfusion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 58e3524ca029b0337f32b2f3773db9be and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices