Taiwan FDA registration c0454defb5c6e0e557a2cca8d2502549
“OsteoMed” primaLOK SP Interspinous Fusion System
TW: “歐特美”普利馬脊突間融合系統
Taiwan·Risk Class 2·MD·OSTEOMED·Registered Nov 16, 2016 – Nov 16, 2021ExpiredRegistration details
- Analysis ID
- c0454defb5c6e0e557a2cca8d2502549
- License Form
- Ministry of Health Medical Device Import No. 029054
- Customs Code
- DHA05602905407
Company information
- Manufacturer
- OSTEOMED
- Manufacturer Country
- United States
- Authorized Representative
- ALSTRONG SCIENTIFIC INTERNATIONAL LTD.
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)
- N3050 Spine correction fixation between the peduncle plates
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 16, 2016
- Expiry Date
- Nov 16, 2021
About this record
Access comprehensive regulatory information for “OsteoMed” primaLOK SP Interspinous 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 c0454defb5c6e0e557a2cca8d2502549 and manufactured by OSTEOMED. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL LTD..
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