Taiwan FDA registration 5a8982e3763bde8e0ee19661d8722808
"Le Pulse" Putt carotid shunt
TW: “樂脈”普特頸動脈分流器
Registration details
- Analysis ID
- 5a8982e3763bde8e0ee19661d8722808
- Customs Code
- DHA00602087601
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
- Apr 01, 2010
- Expiry Date
- Apr 01, 2030
About this record
Access comprehensive regulatory information for "Le Pulse" Putt carotid shunt in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a8982e3763bde8e0ee19661d8722808 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
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