"Zhuangsheng" Vijo mesh - Taiwan Registration 1708ffd6ad9f20c442f54ec118bf4451
Access comprehensive regulatory information for "Zhuangsheng" Vijo mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1708ffd6ad9f20c442f54ec118bf4451 and manufactured by JOHNSON &JOHNSON MEDICAL GMBH;; Johnson & Johnson International, c/o European Logistics Centre. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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
Registration Details
1708ffd6ad9f20c442f54ec118bf4451
DHA00601733802
Product Details
For details, it is Chinese approved copy of the imitation order
I General, Plastic Surgery and Dermatology
I.3300 Surgical mesh
Contract manufacturing;; input
Dates and Status
Oct 05, 2006
Oct 05, 2026

