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“Penumbra” Benchmark Intracranial Access System - Taiwan Registration 3d9b0d90a25b978e5d272a7db7b4bb33

Access comprehensive regulatory information for “Penumbra” Benchmark Intracranial Access System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d9b0d90a25b978e5d272a7db7b4bb33 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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3d9b0d90a25b978e5d272a7db7b4bb33
Registration Details
Taiwan FDA Registration: 3d9b0d90a25b978e5d272a7db7b4bb33
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Device Details

“Penumbra” Benchmark Intracranial Access System
TW: “彼娜波”般馬可顱內通路系統
Risk Class 2
MD

Registration Details

3d9b0d90a25b978e5d272a7db7b4bb33

Ministry of Health Medical Device Import No. 031221

DHA05603122105

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

Jul 24, 2018

Jul 24, 2028