Taiwan FDA registration a9bfdfcc535ab496c886decc0e81937b
Lightning Polymer Composite Material Intervertebral Fusion
TW: 雷特佳高分子複合材料椎間融合器
Taiwan·Risk Class 2·Guanya Biotechnology Co., Ltd. new store factory·Registered Sep 07, 2010 – Sep 07, 2025ExpiredRegistration details
- Analysis ID
- a9bfdfcc535ab496c886decc0e81937b
- Customs Code
- DHY00500309100
Company information
- Manufacturer
- Guanya Biotechnology Co., Ltd. new store factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- A-SPINE Asia 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.3080 椎體間融合裝置
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 07, 2010
- Expiry Date
- Sep 07, 2025
About this record
Access comprehensive regulatory information for Lightning Polymer Composite Material Intervertebral Fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9bfdfcc535ab496c886decc0e81937b and manufactured by Guanya Biotechnology Co., Ltd. new store factory. The authorized representative in Taiwan is A-SPINE Asia 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