"Spite" Juliet lumbar fusion device - Taiwan Registration 4ece3ae09b34e70c0b2dcede67a43fe1

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.