Taiwan FDA registration 2eef00da132dce101f463a16167dc8ad
OSMD Titanium Bone Screw
TW: 沃思坦鈦合金骨釘
Taiwan·Risk Class 2·MD·OSTEOSTANDARD MEDICAL DEVICE CO., LTD.·Registered Sep 30, 2017 – Sep 30, 2027ActiveRegistration details
- Analysis ID
- 2eef00da132dce101f463a16167dc8ad
- License Form
- Ministry of Health Medical Device Manufacturing No. 005908
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
- Sep 30, 2017
- Expiry Date
- Sep 30, 2027
About this record
Access comprehensive regulatory information for OSMD Titanium Bone Screw in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2eef00da132dce101f463a16167dc8ad and manufactured by OSTEOSTANDARD MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is OSTEOSTANDARD MEDICAL DEVICE CO., LTD..
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