Taiwan FDA registration 2cbc3dc54bc5911e12c886b14f91dacc
Antoni lumbar posterior fusion device
TW: 亞東尼腰椎後路融合器
Taiwan·Risk Class 2·SCIENT'X·Registered Aug 18, 2006 – Aug 18, 2016CancelledRegistration details
- Analysis ID
- 2cbc3dc54bc5911e12c886b14f91dacc
- Customs Code
- DHA00601701208
Company information
- Manufacturer
- SCIENT'X
- Manufacturer Country
- France
- Authorized Representative
- CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD.
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.3060 椎體間之脊椎矯正固定物
- Import Information
- import
Dates and status
- Registration Date
- Aug 18, 2006
- Expiry Date
- Aug 18, 2016
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Antoni lumbar posterior fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2cbc3dc54bc5911e12c886b14f91dacc and manufactured by SCIENT'X. The authorized representative in Taiwan is CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD..
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