Taiwan FDA registration 7489780c2ce8f4e0b9df5c40fd27289b
“Arthrex” SutureTak Suture Anchor
TW: “艾思瑞斯”思求太克縫合錨釘
Taiwan·Risk Class 2·MD·ARTHREX, INC.·Registered Apr 25, 2017 – Apr 25, 2027ActiveRegistration details
- Analysis ID
- 7489780c2ce8f4e0b9df5c40fd27289b
- License Form
- Ministry of Health Medical Device Import No. 029649
- Customs Code
- DHA05602964902
Company information
- Manufacturer
- ARTHREX, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
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)
- N3030 Single or multi-metal bone fixation device and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 25, 2017
- Expiry Date
- Apr 25, 2027
About this record
Access comprehensive regulatory information for “Arthrex” SutureTak 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 7489780c2ce8f4e0b9df5c40fd27289b and manufactured by ARTHREX, INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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