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“LENTIS” HydroSmart Posterior Chamber Intraocular Lens with Multifocal Toric Optic - Taiwan Registration bb534a92738341376df96f80916f5e9d

Access comprehensive regulatory information for “LENTIS” HydroSmart Posterior Chamber Intraocular Lens with Multifocal Toric Optic in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bb534a92738341376df96f80916f5e9d and manufactured by Teleon Surgical B.V.. The authorized representative in Taiwan is UNITED MEDICAL INC..

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Registration Details
Taiwan FDA Registration: bb534a92738341376df96f80916f5e9d
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Device Details

“LENTIS” HydroSmart Posterior Chamber Intraocular Lens with Multifocal Toric Optic
TW: "藍提視”多焦點散光人工水晶體
Risk Class 3
MD

Registration Details

bb534a92738341376df96f80916f5e9d

Ministry of Health Medical Device Import No. 026200

DHA05602620003

Company Information

Netherlands

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 22, 2014

Aug 22, 2024