"Ames" Alibet prolapse repair system - Taiwan Registration 4dc19696f85a7a492b5ab1dccf654cf3
Access comprehensive regulatory information for "Ames" Alibet prolapse repair system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4dc19696f85a7a492b5ab1dccf654cf3 and manufactured by AMS Medical Systems Ireland Limited. The authorized representative in Taiwan is KUANPIRE ENTERPRISES CORPORATION.
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
I General, Plastic Surgery and Dermatology
I.3300 Surgical mesh
import
Dates and Status
Aug 25, 2010
Aug 25, 2020
Sep 19, 2018
Cancellation Information
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