“HUMANOPTICS” Acrylic Intraocular Lens_Aspira-aAY - Taiwan Registration fd1528cba4e8f568564fbc0ffd659ba3
Access comprehensive regulatory information for “HUMANOPTICS” Acrylic Intraocular Lens_Aspira-aAY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fd1528cba4e8f568564fbc0ffd659ba3 and manufactured by HumanOptics Holding AG. The authorized representative in Taiwan is MEDBEST ENTERPRISE CO., LTD..
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Device Details
Registration Details
fd1528cba4e8f568564fbc0ffd659ba3
Ministry of Health Medical Device Import No. 033896
DHA05603389605
Product Details
For details, it is Chinese approved copy of the imitation order
M Ophthalmic devices
M3600 intraocular lens
Imported from abroad
Dates and Status
Aug 24, 2020
Aug 24, 2025

