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“Bausch & Lomb” enVista Hydrophobic Toric Acrylic Intraocular Lens - Taiwan Registration 1910001977c86c7a0437c18f54c002b1

Access comprehensive regulatory information for “Bausch & Lomb” enVista Hydrophobic Toric Acrylic 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 1910001977c86c7a0437c18f54c002b1 and manufactured by BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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1910001977c86c7a0437c18f54c002b1
Registration Details
Taiwan FDA Registration: 1910001977c86c7a0437c18f54c002b1
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Device Details

“Bausch & Lomb” enVista Hydrophobic Toric Acrylic Intraocular Lens
TW: “博士倫”恩視非球面散光矯正人工水晶體
Risk Class 3
MD

Registration Details

1910001977c86c7a0437c18f54c002b1

Ministry of Health Medical Device Import No. 028640

DHA05602864002

Company Information

United States

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 21, 2016

Jul 21, 2026