"Spite" Juliet lumbar fusion device
Taiwan·Risk Class 2·SPINEART SA;; ALPES CN SAS·Registered Dec 27, 2018 – Dec 27, 2028Active- Analysis ID
- 6eba4f60ff4a347b2136a3871c6825f9
- Customs Code
- DHA05603193505
- Manufacturer
- SPINEART SA;; ALPES CN SAS
- Manufacturer Country
- France;;Switzerland
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3080 椎體間融合裝置
- Import Information
- import
- Registration Date
- Dec 27, 2018
- Expiry Date
- Dec 27, 2028
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Access comprehensive regulatory information for "Spite" Juliet lumbar fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6eba4f60ff4a347b2136a3871c6825f9 and manufactured by SPINEART SA;; ALPES CN SAS. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SPINEART SA;; ALPES CN SAS, and 1 recent registrations in the same category. 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.