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“Martin” MarSeal vessel sealing - Taiwan Registration ed1ee4bbdbcbdf0edbdceb3bec0911e3

Access comprehensive regulatory information for “Martin” MarSeal vessel sealing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed1ee4bbdbcbdf0edbdceb3bec0911e3 and manufactured by GEBRUDER MARTIN GMBH & CO. KG. The authorized representative in Taiwan is KINDMED CORPORATION.

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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ed1ee4bbdbcbdf0edbdceb3bec0911e3
Registration Details
Taiwan FDA Registration: ed1ee4bbdbcbdf0edbdceb3bec0911e3
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Device Details

“Martin” MarSeal vessel sealing
TW: “瑪珽” 邁斯爾血管閉合器
Risk Class 2
MD
Cancelled

Registration Details

ed1ee4bbdbcbdf0edbdceb3bec0911e3

Ministry of Health Medical Device Import No. 029134

DHA05602913405

Company Information

Product Details

I General and plastic surgical devices

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Dec 07, 2016

Dec 07, 2021

Sep 08, 2023

Cancellation Information

Logged out

未展延而逾期者