Taiwan FDA registration 6872d5018122361b1345603927301ace
“SPINEWAY” TWIN PEAKS Oblique Lumbar Cage
TW: “施百威”腰椎融合器
Taiwan·Risk Class 2·MD·SPINEWAY SA·Registered Feb 17, 2014 – Feb 17, 2024ExpiredRegistration details
- Analysis ID
- 6872d5018122361b1345603927301ace
- License Form
- Ministry of Health Medical Device Import No. 025784
- Customs Code
- DHA05602578401
Company information
- Manufacturer
- SPINEWAY SA
- Manufacturer Country
- France
- Authorized Representative
- SUMMIT BIOMED. 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)
- N3060 Spine correction fixation between vertebral bodies
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 17, 2014
- Expiry Date
- Feb 17, 2024
About this record
Access comprehensive regulatory information for “SPINEWAY” TWIN PEAKS Oblique Lumbar Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6872d5018122361b1345603927301ace and manufactured by SPINEWAY SA. The authorized representative in Taiwan is SUMMIT BIOMED. CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices