Taiwan FDA registration c40433cf046710bf53f09371ae859ac7
"Kuxin" dome hernia mesh
TW: “庫鑫”圓頂疝氣網片
Taiwan·Risk Class 2·COUSIN BIOTECH S.A.S;; COUSIN BIOTECH S.A.S.·Registered Sep 02, 2021 – Sep 02, 2026ActiveRegistration details
- Analysis ID
- c40433cf046710bf53f09371ae859ac7
- Customs Code
- DHA05603493405
Company information
- Manufacturer
- COUSIN BIOTECH S.A.S;; COUSIN BIOTECH S.A.S.
- Manufacturer Country
- France
- Authorized Representative
- Advanced Medical Material Corp.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3300 Surgical mesh
- Import Information
- import
Dates and status
- Registration Date
- Sep 02, 2021
- Expiry Date
- Sep 02, 2026
About this record
Access comprehensive regulatory information for "Kuxin" dome hernia mesh in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c40433cf046710bf53f09371ae859ac7 and manufactured by COUSIN BIOTECH S.A.S;; COUSIN BIOTECH S.A.S.. The authorized representative in Taiwan is Advanced Medical Material Corp..
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