Taiwan FDA registration c3e0ef762313624196a713d8347af8d5
“Arthrex” Arthroscope
TW: “艾思瑞斯”關節鏡
Taiwan·Risk Class 2·MD·Arthrex Inc.·Registered Sep 05, 2017 – Sep 05, 2022ExpiredRegistration details
- Analysis ID
- c3e0ef762313624196a713d8347af8d5
- License Form
- Ministry of Health Medical Device Import No. 030209
- Customs Code
- DHA05603020900
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)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 05, 2017
- Expiry Date
- Sep 05, 2022
About this record
Access comprehensive regulatory information for “Arthrex” Arthroscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c3e0ef762313624196a713d8347af8d5 and manufactured by Arthrex Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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