Taiwan FDA registration 584dd5dab96119ca4bb25fec9ec07604
“SPINEART” JULIET LL Lumbar Cage
TW: “司佰特”茱麗葉腰椎融合器
Taiwan·Risk Class 2·MD·SPINEART SA·Registered Feb 24, 2016 – Feb 24, 2021ExpiredRegistration details
- Analysis ID
- 584dd5dab96119ca4bb25fec9ec07604
- License Form
- Ministry of Health Medical Device Import No. 028208
- Customs Code
- DHA05602820803
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 Orthopedic devices
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 24, 2016
- Expiry Date
- Feb 24, 2021
About this record
Access comprehensive regulatory information for “SPINEART” JULIET LL Lumbar Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 584dd5dab96119ca4bb25fec9ec07604 and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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