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"Gebeike" peelable introduction tube kit - Taiwan Registration 728466d92f6d4d79cd38b992eb46c955

Access comprehensive regulatory information for "Gebeike" peelable introduction tube kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 728466d92f6d4d79cd38b992eb46c955 and manufactured by GREATBATCH MEDICAL INC. The authorized representative in Taiwan is LORION ENTERPRISES INC..

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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728466d92f6d4d79cd38b992eb46c955
Registration Details
Taiwan FDA Registration: 728466d92f6d4d79cd38b992eb46c955
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Device Details

"Gebeike" peelable introduction tube kit
TW: โ€œ่‘›่ฒๅฏโ€ๅฏๅ‰ๅผๅฐŽๅ…ฅ็ฎกๅทฅๅ…ท็ต„
Risk Class 2
Cancelled

Registration Details

728466d92f6d4d79cd38b992eb46c955

DHA00602283405

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1340 Catheter Introducers

import

Dates and Status

Oct 03, 2011

Oct 03, 2021

Oct 12, 2023

Cancellation Information

Logged out

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