Taiwan FDA registration 1708ffd6ad9f20c442f54ec118bf4451
"Zhuangsheng" Vijo mesh
TW: "壯生"薇喬網片
Taiwan·Risk Class 2·JOHNSON &JOHNSON MEDICAL GMBH;; Johnson & Johnson International, c/o European Logistics Centre·Registered Oct 05, 2006 – Oct 05, 2026ActiveRegistration details
- Analysis ID
- 1708ffd6ad9f20c442f54ec118bf4451
- Customs Code
- DHA00601733802
Company information
- Manufacturer
- JOHNSON &JOHNSON MEDICAL GMBH;; Johnson & Johnson International, c/o European Logistics Centre
- Manufacturer Country
- Belgium;;Germany
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3300 Surgical mesh
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Oct 05, 2006
- Expiry Date
- Oct 05, 2026
About this record
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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