Taiwan FDA registration 0724c2f59de0535481ccd41b4312e955
“NuVasive” AttraX Scaffold
TW: “紐瓦索”艾特骨骼填補物
Taiwan·Risk Class 2·MD·NuVasive Inc.·Registered Sep 28, 2021 – Sep 28, 2026ActiveRegistration details
- Analysis ID
- 0724c2f59de0535481ccd41b4312e955
- License Form
- Ministry of Health Medical Device Import No. 034962
- Customs Code
- DHA05603496200
Company information
- Manufacturer
- NuVasive Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MAXIGEN BIOTECH INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3045 Absorbable calcium salt bone cavity filling device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 28, 2021
- Expiry Date
- Sep 28, 2026
About this record
Access comprehensive regulatory information for “NuVasive” AttraX Scaffold in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0724c2f59de0535481ccd41b4312e955 and manufactured by NuVasive Inc.. The authorized representative in Taiwan is MAXIGEN BIOTECH INC..
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