Taiwan FDA registration 648310156a9af060a6c16e9c0f92a6d3
“OSMD” Interlocking Nails System
TW: “沃思坦”骨髓內釘系統
Taiwan·Risk Class 2·MD·OSTEOSTANDARD MEDICAL DEVICE CO., LTD.·Registered Mar 01, 2017 – Mar 01, 2027ActiveRegistration details
- Analysis ID
- 648310156a9af060a6c16e9c0f92a6d3
- License Form
- Ministry of Health Medical Device Manufacturing No. 005707
Company information
- Manufacturer
- OSTEOSTANDARD MEDICAL DEVICE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- OSTEOSTANDARD MEDICAL DEVICE CO., 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)
- N3020 Intra-bone marrow fixation rod
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 01, 2017
- Expiry Date
- Mar 01, 2027
About this record
Access comprehensive regulatory information for “OSMD” Interlocking Nails System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 648310156a9af060a6c16e9c0f92a6d3 and manufactured by OSTEOSTANDARD MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is OSTEOSTANDARD MEDICAL DEVICE CO., LTD..
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