Taiwan FDA registration 94afa3297f73fb933399af99bf6ddf24
"Acerys" post-knee reconstruction system
TW: “艾思瑞斯”膝關節後重建系統
Taiwan·Risk Class 2·ARTHREX INC.·Registered Jan 08, 2008 – Jan 08, 2018CancelledRegistration details
- Analysis ID
- 94afa3297f73fb933399af99bf6ddf24
- Customs Code
- DHA00601853506
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 Orthopedics
- Product Type (Level 2)
- N.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- import
Dates and status
- Registration Date
- Jan 08, 2008
- Expiry Date
- Jan 08, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Acerys" post-knee reconstruction system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94afa3297f73fb933399af99bf6ddf24 and manufactured by ARTHREX INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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