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"Le Pulse" Putt aorta blocks the catheter - Taiwan Registration 81322e7316846942b9bc17d3338c110f

Access comprehensive regulatory information for "Le Pulse" Putt aorta blocks the catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 81322e7316846942b9bc17d3338c110f 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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81322e7316846942b9bc17d3338c110f
Registration Details
Taiwan FDA Registration: 81322e7316846942b9bc17d3338c110f
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Device Details

"Le Pulse" Putt aorta blocks the catheter
TW: โ€œๆจ‚่„ˆโ€ๆ™ฎ็‰นไธปๅ‹•่„ˆ้˜ปๆ–ทๅฐŽ็ฎก
Risk Class 2

Registration Details

81322e7316846942b9bc17d3338c110f

DHA00601988206

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.4450 Vascular clips

import

Dates and Status

Jun 01, 2009

Jun 01, 2029