"Pinabo" Pinabo system - Taiwan Registration 7b3ee143097a1354e6115adfc4a31111
Access comprehensive regulatory information for "Pinabo" Pinabo system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7b3ee143097a1354e6115adfc4a31111 and manufactured by PENUMBRA, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Penumbra, Inc., and 1 recent registrations in the same category. 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.
Device Details
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
Aug 31, 2010
Aug 31, 2020
Jul 15, 2022
Cancellation Information
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