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“OsteoMed” primaLOK FF Facet Fixation System - Taiwan Registration 185eebe1dd3601a3050ac186a5fedd06

Access comprehensive regulatory information for “OsteoMed” primaLOK FF Facet Fixation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 185eebe1dd3601a3050ac186a5fedd06 and manufactured by OSTEOMED. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL LTD..

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185eebe1dd3601a3050ac186a5fedd06
Registration Details
Taiwan FDA Registration: 185eebe1dd3601a3050ac186a5fedd06
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Device Details

“OsteoMed” primaLOK FF Facet Fixation System
TW: “歐特美”普利馬脊椎小面關節固定系統
Risk Class 2
MD

Registration Details

185eebe1dd3601a3050ac186a5fedd06

Ministry of Health Medical Device Import No. 029068

DHA05602906805

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 22, 2016

Nov 22, 2021