Taiwan FDA registration 6afd52d06d129b3da5c47721932ab594
"Schnei-Fai" Taylor external fixture
TW: “史耐輝”泰勒外固定架
Taiwan·Risk Class 2·SMITH & NEPHEW INC, ORTHOPAEDIC DIVISION·Registered Feb 08, 2013 – Feb 08, 2028ActiveRegistration details
- Analysis ID
- 6afd52d06d129b3da5c47721932ab594
- Customs Code
- DHA00602473401
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
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- import
Dates and status
- Registration Date
- Feb 08, 2013
- Expiry Date
- Feb 08, 2028
About this record
Access comprehensive regulatory information for "Schnei-Fai" Taylor external fixture in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6afd52d06d129b3da5c47721932ab594 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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