Taiwan FDA registration fdf94ac7f228fa689b368103328e4acb
“Smith & Nephew” MICRORAPTOR REGENESORB Suture Anchor
TW: “史耐輝”可吸收縫合錨釘
Taiwan·Risk Class 2·MD·SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Registered Jun 02, 2022 – Jun 02, 2027ActiveRegistration details
- Analysis ID
- fdf94ac7f228fa689b368103328e4acb
- License Form
- Ministry of Health Medical Device Import No. 035560
- Customs Code
- DHA05603556008
Company information
- Manufacturer
- SMITH & NEPHEW INC. ENDOSCOPY DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3030 Single or multi-metal bone fixation device and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 02, 2022
- Expiry Date
- Jun 02, 2027
About this record
Access comprehensive regulatory information for “Smith & Nephew” MICRORAPTOR REGENESORB Suture Anchor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdf94ac7f228fa689b368103328e4acb and manufactured by SMITH & NEPHEW INC. ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).
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