Taiwan FDA registration 07107005ba70c238a9dc9a2ca05ab461
“OSMD” Titanium Bone Plate System
TW: “沃思坦”鈦合金骨板系統
Taiwan·Risk Class 2·MD·OSTEOSTANDARD MEDICAL DEVICE CO., LTD.·Registered Dec 05, 2017 – Dec 05, 2027ActiveRegistration details
- Analysis ID
- 07107005ba70c238a9dc9a2ca05ab461
- License Form
- Ministry of Health Medical Device Manufacturing No. 006006
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)
- N3030 Single or multi-metal bone fixation device and accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 05, 2017
- Expiry Date
- Dec 05, 2027
About this record
Access comprehensive regulatory information for “OSMD” Titanium Bone Plate System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 07107005ba70c238a9dc9a2ca05ab461 and manufactured by OSTEOSTANDARD MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is OSTEOSTANDARD MEDICAL DEVICE CO., LTD..
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