Taiwan FDA registration 01515f26495b63283100e79f418feb9a
“VTI” Intervertebral Body Fusion Device
TW: “微堤”椎間融合器
Taiwan·Risk Class 2·MD·NEXT ORTHOSURGICAL·Registered May 05, 2015 – May 05, 2025ExpiredRegistration details
- Analysis ID
- 01515f26495b63283100e79f418feb9a
- License Form
- Ministry of Health Medical Device Import No. 027114
- Customs Code
- DHA05602711402
Company information
- Manufacturer
- NEXT ORTHOSURGICAL
- Manufacturer Country
- United States
- Authorized Representative
- CHEN LIEN SCIENTIFIC 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
- Imported from abroad
Dates and status
- Registration Date
- May 05, 2015
- Expiry Date
- May 05, 2025
About this record
Access comprehensive regulatory information for “VTI” Intervertebral Body Fusion Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 01515f26495b63283100e79f418feb9a and manufactured by NEXT ORTHOSURGICAL. The authorized representative in Taiwan is CHEN LIEN SCIENTIFIC CO., LTD..
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