"Archimi" Haibo intraocular liquid substitutes and accessories - Taiwan Registration b80b53fe06af95d3272759a90578cc1d
Access comprehensive regulatory information for "Archimi" Haibo intraocular liquid substitutes and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number b80b53fe06af95d3272759a90578cc1d and manufactured by AL. CHI.MI.A. S.R.L.. The authorized representative in Taiwan is SUNNY MEDICAL INC..
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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b80b53fe06af95d3272759a90578cc1d
Registration Details
Taiwan FDA Registration: b80b53fe06af95d3272759a90578cc1d
Device Details
"Archimi" Haibo intraocular liquid substitutes and accessories
TW: โ้ฟๅบ็ฑณโๆตทๅ็ผๅ
งๆถฒ้ซๆฟไปฃ็ฉๅ้
ไปถ
Risk Class 3

