"Spite" Romeo Pader interspinal system - Taiwan Registration ac5d217398e6e8fb32f29f080c85df2c
Access comprehensive regulatory information for "Spite" Romeo Pader interspinal system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ac5d217398e6e8fb32f29f080c85df2c 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. 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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ac5d217398e6e8fb32f29f080c85df2c
Registration Details
Taiwan FDA Registration: ac5d217398e6e8fb32f29f080c85df2c
Device Details
"Spite" Romeo Pader interspinal system
TW: โๅธไฝฐ็นโ็พ
ๅฏๆญๅธๅพท่็ช้็ณป็ตฑ
Risk Class 2

