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"Le Pulse" Neotel thrombus removal catheter - Taiwan Registration 1aeacaf94832fc061f8d3d8412d88d3c

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..

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.

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1aeacaf94832fc061f8d3d8412d88d3c
Registration Details
Taiwan FDA Registration: 1aeacaf94832fc061f8d3d8412d88d3c
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Device Details

"Le Pulse" Neotel thrombus removal catheter
TW: โ€œๆจ‚่„ˆโ€ๆ–ฐ็‰น็ˆพ่ก€ๆ “ๆธ…้™คๅฐŽ็ฎก
Risk Class 2

Registration Details

1aeacaf94832fc061f8d3d8412d88d3c

DHA00602231609

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

May 18, 2011

May 18, 2026