Taiwan FDA registration 065514ded46207ea48def0f54e9ac1e5
AVALON Kyphoplasty Kit
TW: 阿凡龍球囊椎體成型術套組
Taiwan·Risk Class 2·MD·Guanya Biotechnology Co., Ltd. new store factory·Registered Dec 02, 2016 – Dec 02, 2026ActiveRegistration details
- Analysis ID
- 065514ded46207ea48def0f54e9ac1e5
- License Form
- Ministry of Health Medical Device Manufacturing No. 005479
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 Orthopedic devices
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 02, 2016
- Expiry Date
- Dec 02, 2026
About this record
Access comprehensive regulatory information for AVALON Kyphoplasty Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 065514ded46207ea48def0f54e9ac1e5 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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