Taiwan FDA registration 07752b10ea2072a7d31580e86d33c051
Redmond Lumbar Cage
TW: 雷蒙腰椎椎間融合器
Taiwan·Risk Class 2·MD·Guanya Biotechnology Co., Ltd. new store factory·Registered Mar 18, 2022 – Mar 18, 2027ActiveRegistration details
- Analysis ID
- 07752b10ea2072a7d31580e86d33c051
- License Form
- Ministry of Health Medical Device Manufacturing No. 007369
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
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 18, 2022
- Expiry Date
- Mar 18, 2027
About this record
Access comprehensive regulatory information for Redmond Lumbar Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 07752b10ea2072a7d31580e86d33c051 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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