Taiwan FDA registration a4b9398d7cf4b199e33c998922fb2e24
"Zhaofeng" bone force lumbar intervertebral fusion device
TW: “兆鋒”骨力腰椎椎間融合器
Taiwan·Risk Class 2·Zhaofeng Biotech Co., Ltd.;; Guanya International Technology Co., Ltd·Registered Nov 27, 2008 – Nov 27, 2013CancelledRegistration details
- Analysis ID
- a4b9398d7cf4b199e33c998922fb2e24
- Customs Code
- DHY00500255501
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Zhaofeng Biotechnology 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
- Nov 27, 2008
- Expiry Date
- Nov 27, 2013
- Cancellation Date
- Aug 10, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Zhaofeng" bone force lumbar intervertebral 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 a4b9398d7cf4b199e33c998922fb2e24 and manufactured by Zhaofeng Biotech Co., Ltd.;; Guanya International Technology Co., Ltd. The authorized representative in Taiwan is Zhaofeng Biotechnology 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