Taiwan FDA registration b88a5c733e96cb18ecb45068acc6d729
“Arthrex” SpeedCinch
TW: “艾思瑞斯”半月軟骨縫合修補器
Taiwan·Risk Class 2·MD·Arthrex Inc.·Registered Apr 12, 2017 – Apr 12, 2022ExpiredRegistration details
- Analysis ID
- b88a5c733e96cb18ecb45068acc6d729
- License Form
- Ministry of Health Medical Device Import No. 029627
- Customs Code
- DHA05602962702
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
- Apr 12, 2017
- Expiry Date
- Apr 12, 2022
About this record
Access comprehensive regulatory information for “Arthrex” SpeedCinch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b88a5c733e96cb18ecb45068acc6d729 and manufactured by Arthrex Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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