Taiwan FDA registration 0c4eb71cf279a1086904c29c803ba31e
Seevert posterior cervical fixation system
TW: 瑟弗特頸椎後路固定系統
Taiwan·Risk Class 2·Guanya Biotechnology Co., Ltd. new store factory·Registered Mar 06, 2015 – Mar 06, 2030ActiveRegistration details
- Analysis ID
- 0c4eb71cf279a1086904c29c803ba31e
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.3070 椎弓螺釘系統
- Import Information
- Domestic
Dates and status
- Registration Date
- Mar 06, 2015
- Expiry Date
- Mar 06, 2030
About this record
Access comprehensive regulatory information for Seevert posterior cervical fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0c4eb71cf279a1086904c29c803ba31e and manufactured by Guanya Biotechnology Co., Ltd. new store factory. The authorized representative in Taiwan is A-SPINE Asia Co., Ltd..
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