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"Zeiss" hydrophobic acrylate posterior chamber intraocular lens - Taiwan Registration ffc4228d098e0eea39bba19776c973dc

Access comprehensive regulatory information for "Zeiss" hydrophobic acrylate posterior chamber 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 ffc4228d098e0eea39bba19776c973dc and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec Production, LLC.. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

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ffc4228d098e0eea39bba19776c973dc
Registration Details
Taiwan FDA Registration: ffc4228d098e0eea39bba19776c973dc
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Device Details

"Zeiss" hydrophobic acrylate posterior chamber intraocular lens
TW: โ€œ่”กๅธโ€็–ๆฐดๆ€งไธ™็ƒฏ้…ธ่„‚ๅพŒๆˆฟไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

ffc4228d098e0eea39bba19776c973dc

DHA05603333606

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.3600 Artificial Crystal

Input;; Contract manufacturing

Dates and Status

Mar 26, 2020

Mar 26, 2025