Taiwan FDA registration b7d2c06a4146acd5408c8742d7c49edd
"Schneihui" Revised intramedullary nail system
TW: "史耐輝" 翻修型髓內釘系統
Taiwan·Risk Class 2·SMITH & NEPHEW INC, ORTHOPAEDIC DIVISION·Registered Dec 27, 2002 – Dec 27, 2017CancelledRegistration details
- Analysis ID
- b7d2c06a4146acd5408c8742d7c49edd
- Customs Code
- DHA00601017106
Company information
- Manufacturer
- SMITH & NEPHEW INC, ORTHOPAEDIC DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3020 骨髓內固定桿
- Import Information
- import
Dates and status
- Registration Date
- Dec 27, 2002
- Expiry Date
- Dec 27, 2017
- 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" Revised 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 b7d2c06a4146acd5408c8742d7c49edd and manufactured by SMITH & NEPHEW INC, ORTHOPAEDIC DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
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