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"Le Pulse" Ihan-Putt carotid shunt - Taiwan Registration 9916437630837345e4b04f466b6b8584

Access comprehensive regulatory information for "Le Pulse" Ihan-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 9916437630837345e4b04f466b6b8584 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.

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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9916437630837345e4b04f466b6b8584
Registration Details
Taiwan FDA Registration: 9916437630837345e4b04f466b6b8584
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Device Details

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

Registration Details

9916437630837345e4b04f466b6b8584

DHA00601967004

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

Feb 20, 2009

Feb 20, 2019

May 19, 2022

Cancellation Information

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