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“LeMaitre” Valvulotome - Taiwan Registration d4a7a7d8ef0e6a121fa2b75552964739

Access comprehensive regulatory information for “LeMaitre” Valvulotome in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d4a7a7d8ef0e6a121fa2b75552964739 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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d4a7a7d8ef0e6a121fa2b75552964739
Registration Details
Taiwan FDA Registration: d4a7a7d8ef0e6a121fa2b75552964739
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Device Details

“LeMaitre” Valvulotome
TW: “樂脈”瓣膜刀
Risk Class 2
MD

Registration Details

d4a7a7d8ef0e6a121fa2b75552964739

Ministry of Health Medical Device Import No. 033956

DHA05603395600

Company Information

United States

Product Details

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

E Cardiovascular devices

E4885 Venous vascular stripper

Imported from abroad

Dates and Status

Sep 16, 2020

Sep 16, 2025