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"Pinabo" embolic ring system - Taiwan Registration e1fc3f06637c1ccf4d706d01930190ea

Access comprehensive regulatory information for "Pinabo" embolic ring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1fc3f06637c1ccf4d706d01930190ea 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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e1fc3f06637c1ccf4d706d01930190ea
Registration Details
Taiwan FDA Registration: e1fc3f06637c1ccf4d706d01930190ea
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Device Details

"Pinabo" embolic ring system
TW: โ€œๅฝผๅจœๆณขโ€ๆ “ๅกž็’ฐ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

e1fc3f06637c1ccf4d706d01930190ea

DHA00602356203

Company Information

United States

Product Details

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

K Neuroscience

K.5950 Artificial embolization device

import

Dates and Status

May 07, 2012

May 07, 2022

Apr 12, 2024

Cancellation Information

Logged out

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