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"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..

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1708ffd6ad9f20c442f54ec118bf4451
Registration Details
Taiwan FDA Registration: 1708ffd6ad9f20c442f54ec118bf4451
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Device Details

"Zhuangsheng" Vijo mesh
TW: "ๅฃฏ็”Ÿ"่–‡ๅ–ฌ็ถฒ็‰‡
Risk Class 2

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