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“Penumbra” Delivery Microcatheters - Taiwan Registration 91f2118481d49185f7779da26f30dc8f

Access comprehensive regulatory information for “Penumbra” Delivery Microcatheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 91f2118481d49185f7779da26f30dc8f and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL 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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91f2118481d49185f7779da26f30dc8f
Registration Details
Taiwan FDA Registration: 91f2118481d49185f7779da26f30dc8f
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Device Details

“Penumbra” Delivery Microcatheters
TW: “彼娜波”輸送微導管
Risk Class 2
MD

Registration Details

91f2118481d49185f7779da26f30dc8f

Ministry of Health Medical Device Import No. 026140

DHA05602614001

Company Information

United States

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

May 06, 2014

May 06, 2024