Taiwan FDA registration 4b66bd7b63c7e2f313fa0fec16dc7088
"Osto" bone density analysis instrument
TW: “澳思托” 骨質密度分析儀
Taiwan·Risk Class 2·OsteoSys Co., Ltd·Registered Oct 28, 2024 – Oct 28, 2029ActiveRegistration details
- Analysis ID
- 4b66bd7b63c7e2f313fa0fec16dc7088
- Customs Code
- DHAS5603745302
Company information
- Manufacturer
- OsteoSys Co., Ltd
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- GREENEVER MEDICAL SYSTEMS INC .
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1170 骨密度分析儀
- Import Information
- Input;; The consent of the Nuclear Safety Commission must be obtained for each import of this medical device.
Dates and status
- Registration Date
- Oct 28, 2024
- Expiry Date
- Oct 28, 2029
About this record
Access comprehensive regulatory information for "Osto" bone density analysis instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b66bd7b63c7e2f313fa0fec16dc7088 and manufactured by OsteoSys Co., Ltd. The authorized representative in Taiwan is GREENEVER MEDICAL SYSTEMS INC ..
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