Taiwan FDA registration 0c09f802888ae88c55e516ec1d682f6d
“OSMD” Polyether Ether Ketone Interbody Fusion Cage
TW: “沃思坦”聚醚醚酮椎間融合器
Taiwan·Risk Class 2·MD·OSTEOSTANDARD MEDICAL DEVICE CO., LTD.·Registered Aug 18, 2019 – Aug 18, 2024ExpiredRegistration details
- Analysis ID
- 0c09f802888ae88c55e516ec1d682f6d
- License Form
- Ministry of Health Medical Device Manufacturing No. 006522
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)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 18, 2019
- Expiry Date
- Aug 18, 2024
About this record
Access comprehensive regulatory information for “OSMD” Polyether Ether Ketone Interbody Fusion Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0c09f802888ae88c55e516ec1d682f6d and manufactured by OSTEOSTANDARD MEDICAL DEVICE CO., LTD.. The authorized representative in Taiwan is OSTEOSTANDARD MEDICAL DEVICE CO., LTD..
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