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"Zeiss" Lisa trifocal hydrophilic posterior chamber intraocular lens - Taiwan Registration a3abb12b4d2cdf48c59ae608310bf8c3

Access comprehensive regulatory information for "Zeiss" Lisa trifocal 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 a3abb12b4d2cdf48c59ae608310bf8c3 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 SAS, 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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a3abb12b4d2cdf48c59ae608310bf8c3
Registration Details
Taiwan FDA Registration: a3abb12b4d2cdf48c59ae608310bf8c3
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Device Details

"Zeiss" Lisa trifocal hydrophilic posterior chamber intraocular lens
TW: โ€œ่”กๅธโ€้บ—่ŽŽไธ‰็„ฆ้ปž่ฆชๆฐดๆ€งๅพŒๆˆฟไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

a3abb12b4d2cdf48c59ae608310bf8c3

DHA05603394607

Company Information

Product Details

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

M Ophthalmology

M.3600 Artificial Crystal

Contract manufacturing;; input

Dates and Status

Sep 09, 2020

Sep 09, 2025

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