Taiwan FDA registration 0577c8014b9f6f36099446efabaaac49
“SPINEART” ROMEO 2 Lumbar Posterior Osteosynthesis System
TW: “司佰特”羅密歐腰椎後路固定系統
Taiwan·Risk Class 2·MD·SPINEART SA·Registered Sep 08, 2020 – Sep 08, 2025ExpiredRegistration details
- Analysis ID
- 0577c8014b9f6f36099446efabaaac49
- License Form
- Ministry of Health Medical Device Import No. 033853
- Customs Code
- DHA05603385300
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)
- N3070 Pedicle screw system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 08, 2020
- Expiry Date
- Sep 08, 2025
About this record
Access comprehensive regulatory information for “SPINEART” ROMEO 2 Lumbar Posterior Osteosynthesis System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0577c8014b9f6f36099446efabaaac49 and manufactured by SPINEART SA. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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