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"Pinabo" Nuno intracranial delivery system - Taiwan Registration dae9fcd97704ee00097681eb7883517c

Access comprehensive regulatory information for "Pinabo" Nuno intracranial delivery system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dae9fcd97704ee00097681eb7883517c 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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dae9fcd97704ee00097681eb7883517c
Registration Details
Taiwan FDA Registration: dae9fcd97704ee00097681eb7883517c
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Device Details

"Pinabo" Nuno intracranial delivery system
TW: โ€œๅฝผๅจœๆณขโ€ ็ด่ซพ้กฑๅ…งๅฐŽๅ…ฅ็ณป็ตฑ
Risk Class 2

Registration Details

dae9fcd97704ee00097681eb7883517c

DHA05603677600

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Dec 11, 2023

Dec 11, 2028