Taiwan FDA registration 185eebe1dd3601a3050ac186a5fedd06
“OsteoMed” primaLOK FF Facet Fixation System
TW: “歐特美”普利馬脊椎小面關節固定系統
Taiwan·Risk Class 2·MD·OSTEOMED·Registered Nov 22, 2016 – Nov 22, 2021ExpiredRegistration details
- Analysis ID
- 185eebe1dd3601a3050ac186a5fedd06
- License Form
- Ministry of Health Medical Device Import No. 029068
- Customs Code
- DHA05602906805
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 22, 2016
- Expiry Date
- Nov 22, 2021
About this record
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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