Taiwan FDA registration 9225678dee85099cb3ba71cdb0ee3ee4
"Adir" posterior lumbar fusion device
TW: “艾迪爾”後方腰椎融合器
Taiwan·Risk Class 2·LDR Medical·Registered Jul 06, 2013 – Jul 06, 2018CancelledRegistration details
- Analysis ID
- 9225678dee85099cb3ba71cdb0ee3ee4
- Customs Code
- DHA00602516707
Company information
- Manufacturer
- LDR Medical
- Manufacturer Country
- France
- Authorized Representative
- HOLLING BIO-PHARMA. CORP.
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
- Jul 06, 2013
- Expiry Date
- Jul 06, 2018
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Adir" posterior lumbar 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 9225678dee85099cb3ba71cdb0ee3ee4 and manufactured by LDR Medical. The authorized representative in Taiwan is HOLLING BIO-PHARMA. CORP..
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