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"Le Pulse" remote perfusion catheter - Taiwan Registration 58e3524ca029b0337f32b2f3773db9be

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.

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58e3524ca029b0337f32b2f3773db9be
Registration Details
Taiwan FDA Registration: 58e3524ca029b0337f32b2f3773db9be
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Device Details

"Le Pulse" remote perfusion catheter
TW: โ€œๆจ‚่„ˆโ€้ ็ซฏ็ŒๆตๅฐŽ็ฎก
Risk Class 2

Registration Details

58e3524ca029b0337f32b2f3773db9be

DHA00601879700

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing

import

Dates and Status

Apr 15, 2008

Apr 15, 2028