Taiwan FDA registration 6d5719d8ab5805c2b9084d7116a0ceec
"Spite" Romeo lumbar posterior fusion system
TW: “司佰特”羅蜜歐腰椎後路融合系統
Taiwan·Risk Class 2·SPINEART SA·Registered Sep 15, 2010 – Sep 15, 2020CancelledRegistration details
- Analysis ID
- 6d5719d8ab5805c2b9084d7116a0ceec
- Customs Code
- DHA00602146100
Company information
- Manufacturer
- SPINEART SA
- Manufacturer Country
- Switzerland
- 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.3070 椎弓螺釘系統
- Import Information
- import
Dates and status
- Registration Date
- Sep 15, 2010
- Expiry Date
- Sep 15, 2020
- 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 "Spite" Romeo lumbar posterior fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6d5719d8ab5805c2b9084d7116a0ceec and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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