"Fidia" Al vitreous replacement - Taiwan Registration c41960f84af1c611fa705024b8ee44dc
Access comprehensive regulatory information for "Fidia" Al vitreous replacement in Taiwan's medical device market through Pure Global AI's free database. is registered under number c41960f84af1c611fa705024b8ee44dc and manufactured by FIDIA FARMACEUTICI S.P.A.. The authorized representative in Taiwan is MED PHARMA CO., 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
Suitable for use in anterior or posterior chamber surgery and removed before surgery is completed.
M Ophthalmology
import
Dates and Status
Jan 18, 2002
Jan 18, 2007
Nov 09, 2012
Cancellation Information
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