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“OsteoMed” primaLOK SP Interspinous Fusion System - Taiwan Registration c0454defb5c6e0e557a2cca8d2502549

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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c0454defb5c6e0e557a2cca8d2502549
Registration Details
Taiwan FDA Registration: c0454defb5c6e0e557a2cca8d2502549
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Device Details

“OsteoMed” primaLOK SP Interspinous Fusion System
TW: “歐特美”普利馬脊突間融合系統
Risk Class 2
MD

Registration Details

c0454defb5c6e0e557a2cca8d2502549

Ministry of Health Medical Device Import No. 029054

DHA05602905407

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3050 Spine correction fixation between the peduncle plates

Imported from abroad

Dates and Status

Nov 16, 2016

Nov 16, 2021