"Spite" Juliet lumbar fusion device
Taiwan·Risk Class 2·SPINEART SA;; ALPES CN SAS·Registered Sep 07, 2011 – Sep 07, 2026Active- Analysis ID
- 4ece3ae09b34e70c0b2dcede67a43fe1
- Customs Code
- DHA00602277604
- 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.3060 椎體間之脊椎矯正固定物
- Import Information
- import
- Registration Date
- Sep 07, 2011
- Expiry Date
- Sep 07, 2026
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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 4ece3ae09b34e70c0b2dcede67a43fe1 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.