Taiwan FDA registration f94a4802c86d137fea00a33511a12a50
"Schneihui" Moore artificial femur
TW: “史耐輝”摩爾人工股骨
Taiwan·Risk Class 2·SMITH & NEPHEW ORTHOPAEDICS GMBH·Registered Dec 14, 2009 – Dec 14, 2019CancelledRegistration details
- Analysis ID
- f94a4802c86d137fea00a33511a12a50
- Customs Code
- DHA00602048101
Company information
- Manufacturer
- SMITH & NEPHEW ORTHOPAEDICS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3360 Condylar jointed femoral (hemicondyle) metal bone cement or cementless cement-type supplement
- Import Information
- import
Dates and status
- Registration Date
- Dec 14, 2009
- Expiry Date
- Dec 14, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Schneihui" Moore artificial femur in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f94a4802c86d137fea00a33511a12a50 and manufactured by SMITH & NEPHEW ORTHOPAEDICS GMBH. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
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