"Nidek" diode laser solidifier - Taiwan Registration 8dfa963418c020382ac08b55f8eecf8f
Access comprehensive regulatory information for "Nidek" diode laser solidifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8dfa963418c020382ac08b55f8eecf8f and manufactured by NIDEK CO., LTD.. The authorized representative in Taiwan is IKI MEDICAL 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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8dfa963418c020382ac08b55f8eecf8f
Registration Details
Taiwan FDA Registration: 8dfa963418c020382ac08b55f8eecf8f
Device Details
"Nidek" diode laser solidifier
TW: "ๅฐผๅพทๅ
"ไบๆฅต้ซ้ทๅฐๅ
ๅๅบๅ
Risk Class 2
Cancelled

