Taiwan FDA registration 25a4d19ccc40984f87c749f0542a4771
“Smith & Nephew” Journey II TKA Total Knee System
TW: “史耐輝”全膝關節系統
Taiwan·Risk Class 2·MD·Smith & Nephew, Inc.·Registered May 01, 2023 – May 01, 2028ActiveRegistration details
- Analysis ID
- 25a4d19ccc40984f87c749f0542a4771
- License Form
- Ministry of Health Medical Device Import No. 036489
- Customs Code
- DHA05603648907
Company information
- Manufacturer
- Smith & Nephew, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3560 Semi-restrictive knee femoral tibial polymer/metal/polymeric cement compound
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 01, 2023
- Expiry Date
- May 01, 2028
About this record
Access comprehensive regulatory information for “Smith & Nephew” Journey II TKA Total Knee System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25a4d19ccc40984f87c749f0542a4771 and manufactured by Smith & Nephew, Inc.. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
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