Pure Global

"Le Pulse" arterial thrombus clearance catheter - Taiwan Registration 2e2a8679304ba7ec8bcef19bec75435f

Access comprehensive regulatory information for "Le Pulse" arterial thrombus clearance catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2e2a8679304ba7ec8bcef19bec75435f 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 Database
Powered by Pure Global AI
89,000+ Devices
2e2a8679304ba7ec8bcef19bec75435f
Registration Details
Taiwan FDA Registration: 2e2a8679304ba7ec8bcef19bec75435f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Le Pulse" arterial thrombus clearance catheter
TW: โ€œๆจ‚่„ˆโ€ๅ‹•่„ˆ่ก€ๆ “ๆธ…้™คๅฐŽ็ฎก
Risk Class 2

Registration Details

2e2a8679304ba7ec8bcef19bec75435f

DHA00601881502

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.5150 ่ก€ๆ “ๅˆ‡้™ค่ก“ๅฐŽ็ฎก

import

Dates and Status

Apr 24, 2008

Apr 24, 2028