Taiwan FDA registration aa719566b7e8e391cd6740cc1826cf39
"Schneihui" forearm interlocking intramedullary nail system
TW: "史耐輝" 前臂交鎖髓內釘系統
Taiwan·Risk Class 2·SMITH & NEPHEW INC, ORTHOPAEDIC DIVISION·Registered Jun 19, 2003 – Jun 19, 2018CancelledRegistration details
- Analysis ID
- aa719566b7e8e391cd6740cc1826cf39
- Customs Code
- DHA00601032102
Company information
- Manufacturer
- SMITH & NEPHEW INC, ORTHOPAEDIC DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Jun 19, 2003
- Expiry Date
- Jun 19, 2018
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Schneihui" forearm interlocking intramedullary nail system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa719566b7e8e391cd6740cc1826cf39 and manufactured by SMITH & NEPHEW INC, ORTHOPAEDIC DIVISION. 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