Taiwan FDA registration 9c5997b18cb601fe7d7b46890bda69c9
"Vitron" polymer composite/titanium alloy material intervertebral fusion system
TW: “威創”高分子複合/鈦合金材料椎間融合系統
Taiwan·Risk Class 2·Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory·Registered Mar 30, 2011 – Mar 09, 2026ExpiredRegistration details
- Analysis ID
- 9c5997b18cb601fe7d7b46890bda69c9
- Customs Code
- DHY00500328003
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WILTROM CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3060 椎體間之脊椎矯正固定物
- Import Information
- Domestic
Dates and status
- Registration Date
- Mar 30, 2011
- Expiry Date
- Mar 09, 2026
About this record
Access comprehensive regulatory information for "Vitron" polymer composite/titanium alloy material intervertebral fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c5997b18cb601fe7d7b46890bda69c9 and manufactured by Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is WILTROM 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