Taiwan FDA registration e047e632904b68081ba8550a8effb618
"Aceris" anterior cruciate ligament reconstruction system
TW: “艾思瑞斯”前十字韌帶重建系統
Taiwan·Risk Class 2·ARTHREX INC.·Registered Jun 26, 2007 – Jun 26, 2022CancelledRegistration details
- Analysis ID
- e047e632904b68081ba8550a8effb618
- Customs Code
- DHA00601814101
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.3040 Smooth or spiral metal bone fixations
- Import Information
- import
Dates and status
- Registration Date
- Jun 26, 2007
- Expiry Date
- Jun 26, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aceris" anterior cruciate ligament 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 e047e632904b68081ba8550a8effb618 and manufactured by ARTHREX INC.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices