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"Le Pulse" Putt carotid shunt - Taiwan Registration 5a8982e3763bde8e0ee19661d8722808

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.

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5a8982e3763bde8e0ee19661d8722808
Registration Details
Taiwan FDA Registration: 5a8982e3763bde8e0ee19661d8722808
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Device Details

"Le Pulse" Putt carotid shunt
TW: โ€œๆจ‚่„ˆโ€ๆ™ฎ็‰น้ ธๅ‹•่„ˆๅˆ†ๆตๅ™จ
Risk Class 2

Registration Details

5a8982e3763bde8e0ee19661d8722808

DHA00602087601

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

Apr 01, 2010

Apr 01, 2030