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"Mueryan" Errui intraocular lens - Taiwan Registration 118398d17d7bdd0d914d5c1bf730409d

Access comprehensive regulatory information for "Mueryan" Errui 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 118398d17d7bdd0d914d5c1bf730409d and manufactured by MORCHER GMBH. The authorized representative in Taiwan is HEALTH CARE MEDICAL INC..

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118398d17d7bdd0d914d5c1bf730409d
Registration Details
Taiwan FDA Registration: 118398d17d7bdd0d914d5c1bf730409d
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Device Details

"Mueryan" Errui intraocular lens
TW: โ€œ็›ฎ็ˆพ่‰ทโ€ๆ„›่Šฎไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3
Cancelled

Registration Details

118398d17d7bdd0d914d5c1bf730409d

DHA00602179108

Company Information

Germany

Product Details

Used to replace normal lentles or patients requiring iridescent reconstruction in the following described cases, such as: 1. congenital or acquired anisis, 2. traumatic aniridia, 3. partial absence of iris, 4. albinism (congenital pigment deficiency). (This product is not required for cataract or alens patients).

M Ophthalmology

import

Dates and Status

Dec 14, 2010

Dec 14, 2025

Sep 15, 2023

Cancellation Information

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