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“Valeant Med” FOCUSforce ULTRAflex Spheric Intraocular Lens - Taiwan Registration 0c09fd251eedfc599f15815982d1047e

Access comprehensive regulatory information for “Valeant Med” FOCUSforce ULTRAflex Spheric Intraocular Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0c09fd251eedfc599f15815982d1047e and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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0c09fd251eedfc599f15815982d1047e
Registration Details
Taiwan FDA Registration: 0c09fd251eedfc599f15815982d1047e
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Device Details

“Valeant Med” FOCUSforce ULTRAflex Spheric Intraocular Lens
TW: “威朗”博科視單片式球面人工水晶體
Risk Class 3
MD

Registration Details

0c09fd251eedfc599f15815982d1047e

Ministry of Health Medical Device Import No. 029976

DHA05602997601

Company Information

Poland

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

Jul 19, 2017

Jul 19, 2022