"Aiwei Medicine" Aiwei Modified Guide Tube - Taiwan Registration 7384d954420a19d58f7187c2a8db97d9
Access comprehensive regulatory information for "Aiwei Medicine" Aiwei Modified 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 7384d954420a19d58f7187c2a8db97d9 and manufactured by ALVIMEDICA TฤฐBBฤฐ Urunler SAN. AND EXTERNAL. T.C. Inc.. The authorized representative in Taiwan is JENS MEDICAL CONSULTING LTD..
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.
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 08, 2013
Jul 08, 2018
Aug 05, 2022
Cancellation Information
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