Taiwan FDA registration 83bcc1e386c0754411825040ce351daa
“Arthrex” Corkscrew Suture Anchor
TW: “艾思瑞斯”闊克思固縫合錨釘
Taiwan·Risk Class 2·MD·ARTHREX, INC.·Registered Aug 16, 2016 – Aug 16, 2026ActiveRegistration details
- Analysis ID
- 83bcc1e386c0754411825040ce351daa
- License Form
- Ministry of Health Medical Device Import No. 028733
- Customs Code
- DHA05602873309
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)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 16, 2016
- Expiry Date
- Aug 16, 2026
About this record
Access comprehensive regulatory information for “Arthrex” Corkscrew 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 83bcc1e386c0754411825040ce351daa and manufactured by ARTHREX, INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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