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"Zeiss" esfinafil spherical hydrophilic posterior chamber intraocular lens - Taiwan Registration 26edcaec519ecc6d69d16c850fcc204c

Access comprehensive regulatory information for "Zeiss" esfinafil spherical hydrophilic 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 26edcaec519ecc6d69d16c850fcc204c and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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26edcaec519ecc6d69d16c850fcc204c
Registration Details
Taiwan FDA Registration: 26edcaec519ecc6d69d16c850fcc204c
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Device Details

"Zeiss" esfinafil spherical hydrophilic posterior chamber intraocular lens
TW: โ€œ่”กๅธโ€่‰พๆ–ฏ่ฒ้‚ฃ้ž็ƒ้ข่ฆชๆฐดๆ€งๅพŒๆˆฟไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

26edcaec519ecc6d69d16c850fcc204c

DHA05603394505

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

Sep 09, 2020

Sep 09, 2025

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