Taiwan FDA registration 0475109caf6563d5fc6bee0bfcd38e67
“Arthrex” Meniscal Cinch II
TW: “艾思瑞斯”半月軟骨縫合修補器
Taiwan·Risk Class 2·MD·ARTHREX, INC.·Registered Nov 21, 2019 – Nov 21, 2024ExpiredRegistration details
- Analysis ID
- 0475109caf6563d5fc6bee0bfcd38e67
- License Form
- Ministry of Health Medical Device Import No. 033006
- Customs Code
- DHA05603300601
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)
- I General and plastic surgical devices
- Product Type (Level 2)
- I5000 Non-absorbable polyethylene suture
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 21, 2019
- Expiry Date
- Nov 21, 2024
About this record
Access comprehensive regulatory information for “Arthrex” Meniscal Cinch II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0475109caf6563d5fc6bee0bfcd38e67 and manufactured by ARTHREX, INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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