Taiwan FDA registration cd578e135cb0db1f35ec507d8dcf374a
Titanium subvertebral fixation system
TW: 鈦亞脊椎固定系統
Taiwan·Risk Class 2·JBone Biotechnology Co.,Ltd.·Registered Mar 18, 2022 – Mar 18, 2027ActiveRegistration details
- Analysis ID
- cd578e135cb0db1f35ec507d8dcf374a
Company information
- Manufacturer
- JBone Biotechnology Co.,Ltd.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JBone Biotechnology Co.,Ltd.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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 18, 2022
- Expiry Date
- Mar 18, 2027
About this record
Access comprehensive regulatory information for Titanium subvertebral 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 cd578e135cb0db1f35ec507d8dcf374a and manufactured by JBone Biotechnology Co.,Ltd.. The authorized representative in Taiwan is JBone 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.
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