Ganak Pushima pelvic floor repair system - Taiwan Registration 8f730074ec100f48e6231a3e9b0ebb37
Access comprehensive regulatory information for Ganak Pushima pelvic floor 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 8f730074ec100f48e6231a3e9b0ebb37 and manufactured by ETHICON SARL. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.
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
Jun 30, 2010
Jun 30, 2015
Jan 15, 2015
Cancellation Information
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