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“LeMaitre” Aortic Occlusion Catheter - Taiwan Registration e70f89f8880acbe5972779d5e0ea8e90

Access comprehensive regulatory information for “LeMaitre” Aortic Occlusion Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e70f89f8880acbe5972779d5e0ea8e90 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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e70f89f8880acbe5972779d5e0ea8e90
Registration Details
Taiwan FDA Registration: e70f89f8880acbe5972779d5e0ea8e90
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Device Details

“LeMaitre” Aortic Occlusion Catheter
TW: “樂脈”主動脈阻斷導管
Risk Class 2
MD

Registration Details

e70f89f8880acbe5972779d5e0ea8e90

Ministry of Health Medical Device Import No. 034072

DHA05603407203

Company Information

United States

Product Details

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

E Cardiovascular devices

E4450 Vascular Clip

Imported from abroad

Dates and Status

Nov 05, 2020

Nov 05, 2025