"Ames" light mesh prolapse repair system - Taiwan Registration ec5da38766204d9c264178fddb056bde
Access comprehensive regulatory information for "Ames" light mesh 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 ec5da38766204d9c264178fddb056bde 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
Sep 08, 2008
Sep 08, 2018
Jun 07, 2022
Cancellation Information
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