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"Ostic" Atishen amorphous intraocular lens - Taiwan Registration a7e2aab9a8bf9af5e406caaa242945a9

Access comprehensive regulatory information for "Ostic" Atishen amorphous 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 a7e2aab9a8bf9af5e406caaa242945a9 and manufactured by OPHTEC B.V.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.

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a7e2aab9a8bf9af5e406caaa242945a9
Registration Details
Taiwan FDA Registration: a7e2aab9a8bf9af5e406caaa242945a9
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Device Details

"Ostic" Atishen amorphous intraocular lens
TW: โ€œๆญๆ–ฏๆๅ…‹โ€้˜ฟๆ็”ณ็„กๆ™ถ้ซ”ๅผไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

a7e2aab9a8bf9af5e406caaa242945a9

DHA00602071003

Company Information

Netherlands

Product Details

Amorphous patients with insufficient posterior capsule support to place posterior chamber intraocular lenses.

M Ophthalmology

import

Dates and Status

Jun 15, 2010

Jun 15, 2025