Taiwan FDA registration b49bc0938681a4d7a2bd85a232f9bbb0

"Zhuangsheng" Fly Silkle part absorbable mesh

TW: “壯生”飛絲樂部份可吸收網片
Taiwan flagTaiwan·Risk Class 2·JOHNSON & JOHNSON MEDICAL GMBH;; Johnson & Johnson International, c/o European Logistics Centre·Registered Oct 18, 2011 – Oct 18, 2021Cancelled
Registration details
Analysis ID
b49bc0938681a4d7a2bd85a232f9bbb0
Customs Code
DHA00602295300
Company information
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
Input;; Contract manufacturing
Dates and status
Registration Date
Oct 18, 2011
Expiry Date
Oct 18, 2021
Cancellation Date
Dec 14, 2021
Cancellation information
Status
Logged out
Reason
許可證已逾有效期;;自請註銷
About this record

Access comprehensive regulatory information for "Zhuangsheng" Fly Silkle part absorbable mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b49bc0938681a4d7a2bd85a232f9bbb0 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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