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"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..

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b80b53fe06af95d3272759a90578cc1d
Registration Details
Taiwan FDA Registration: b80b53fe06af95d3272759a90578cc1d
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Device Details

"Archimi" Haibo intraocular liquid substitutes and accessories
TW: โ€œ้˜ฟๅŸบ็ฑณโ€ๆตทๅš็œผๅ…งๆถฒ้ซ”ๆ›ฟไปฃ็‰ฉๅŠ้…ไปถ
Risk Class 3

Registration Details

b80b53fe06af95d3272759a90578cc1d

DHA00602314500

Company Information

Italy

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.4275 ็œผๅ…งๅ……ๅกซ็”จๆถฒ้ซ”

import

Dates and Status

Dec 23, 2011

Dec 23, 2026