Taiwan FDA registration 543d289c7cf4b80d24f89062be9c7f12
“Smith & Nephew” Biolox delta ceramic femoral components
TW: “史耐輝”陶瓷股骨組件
Registration details
- Analysis ID
- 543d289c7cf4b80d24f89062be9c7f12
- License Form
- Ministry of Health Medical Device Import No. 027168
- Customs Code
- DHA05602716802
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 Orthopedic devices
- Product Type (Level 2)
- N3353 Metal/ceramic/polymer bone cement or non-porous coated cement-free cement compound for semi-restricted hip joints
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 24, 2015
- Expiry Date
- Apr 24, 2025
About this record
Access comprehensive regulatory information for “Smith & Nephew” Biolox delta ceramic femoral components in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 543d289c7cf4b80d24f89062be9c7f12 and manufactured by SMITH & NEPHEW ORTHOPAEDICS GMBH. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices