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"Le Pulse" Put-Ihan carotid shunt - Taiwan Registration d6c18cf73aa9da0a3500d24213e4679d

Access comprehensive regulatory information for "Le Pulse" Put-Ihan 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 d6c18cf73aa9da0a3500d24213e4679d 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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d6c18cf73aa9da0a3500d24213e4679d
Registration Details
Taiwan FDA Registration: d6c18cf73aa9da0a3500d24213e4679d
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Device Details

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

Registration Details

d6c18cf73aa9da0a3500d24213e4679d

DHA00601885205

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

May 12, 2008

May 12, 2023