Taiwan FDA registration 6ea1ad1756032f4c4ac6b90d537cc0e5
“Megaspine” Alive Spinal Spacer System
TW: “兆峰”艾力弗脊椎椎間穩定系統
Taiwan·Risk Class 2·MD·MEGASPINE MEDICAL CO., LTD.·Registered Sep 01, 2017 – Sep 01, 2027ActiveRegistration details
- Analysis ID
- 6ea1ad1756032f4c4ac6b90d537cc0e5
- License Form
- Ministry of Health Medical Device Manufacturing No. 005896
Company information
- Manufacturer
- MEGASPINE MEDICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MEGASPINE MEDICAL 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
- Sep 01, 2017
- Expiry Date
- Sep 01, 2027
About this record
Access comprehensive regulatory information for “Megaspine” Alive Spinal Spacer System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ea1ad1756032f4c4ac6b90d537cc0e5 and manufactured by MEGASPINE MEDICAL CO., LTD.. The authorized representative in Taiwan is MEGASPINE MEDICAL CO., LTD..
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