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"Pinabo" microcatheter - Taiwan Registration 61c171096a2bd393b266a3d2e278dba9

Access comprehensive regulatory information for "Pinabo" microcatheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61c171096a2bd393b266a3d2e278dba9 and manufactured by PENUMBRA, 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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61c171096a2bd393b266a3d2e278dba9
Registration Details
Taiwan FDA Registration: 61c171096a2bd393b266a3d2e278dba9
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Device Details

"Pinabo" microcatheter
TW: โ€œๅฝผๅจœๆณขโ€ๅพฎๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

61c171096a2bd393b266a3d2e278dba9

DHA00602330904

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Mar 29, 2012

Mar 29, 2017

Nov 26, 2019

Cancellation Information

Logged out

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