"Medtronic" Sherpa guide tube - Taiwan Registration fe8e09ce7ce7773f9ac5e4d284f3fcec
Access comprehensive regulatory information for "Medtronic" Sherpa guide tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe8e09ce7ce7773f9ac5e4d284f3fcec and manufactured by MEDTRONIC VASCULAR. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC VASCULAR, 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
Jul 04, 2008
Jul 04, 2023
Jan 08, 2020
Cancellation Information
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