"Pinabo" Pinabo system - Taiwan Registration 938dc7c6b1b776448d64da3f9a40942f
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 938dc7c6b1b776448d64da3f9a40942f 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
Details are as detailed as approved Chinese instructions
K Neuroscience
K.5600 Neurovascular mechanical clot removal device for the treatment of acute ischemic stroke
import
Dates and Status
Jan 06, 2023
Jan 06, 2028