Taiwan FDA registration 6d9008f08d5f1b934364b887f5ff458d
“Arthrex” FiberTak suture anchor
TW: “艾思瑞斯”凡博太克縫合錨釘
Taiwan·Risk Class 2·MD·Arthrex Inc.·Registered Jul 25, 2017 – Jul 25, 2027ActiveRegistration details
- Analysis ID
- 6d9008f08d5f1b934364b887f5ff458d
- License Form
- Ministry of Health Medical Device Import No. 030021
- Customs Code
- DHA05603002105
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
- Jul 25, 2017
- Expiry Date
- Jul 25, 2027
About this record
Access comprehensive regulatory information for “Arthrex” FiberTak 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 6d9008f08d5f1b934364b887f5ff458d and manufactured by Arthrex Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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