Taiwan FDA registration a69616d899f68007ef1e8f0e10de79f9
JBone Interbody Fusion Device System
TW: 健寶椎間融合器系統
Taiwan·Risk Class 2·MD·JBone Biotechnology Co.,Ltd.·Registered Feb 02, 2023 – Feb 02, 2028ActiveRegistration details
- Analysis ID
- a69616d899f68007ef1e8f0e10de79f9
- License Form
- Ministry of Health Medical Device Manufacturing No. 007727
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)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 02, 2023
- Expiry Date
- Feb 02, 2028
About this record
Access comprehensive regulatory information for JBone Interbody Fusion Device System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a69616d899f68007ef1e8f0e10de79f9 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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