Taiwan FDA registration 3319a75e0b03de65e10b0bf9d84ae1ee

"Zeiss" Lisa trifocal astigmatism corrects hydrophilic posterior chamber intraocular lenses

TW: “蔡司”麗莎三焦點散光矯正親水性後房人工水晶體
Taiwan flagTaiwan·Risk Class 3·CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG·Registered Dec 16, 2021 – Dec 16, 2026Active
Registration details
Analysis ID
3319a75e0b03de65e10b0bf9d84ae1ee
Customs Code
DHA05603511401
Company information
Manufacturer Country
Germany
Authorized Representative
Carl Zeiss Co., Ltd. Taipei Branch
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.3600 Artificial Crystal
Import Information
import
Dates and status
Registration Date
Dec 16, 2021
Expiry Date
Dec 16, 2026
About this record

Access comprehensive regulatory information for "Zeiss" Lisa trifocal astigmatism corrects hydrophilic posterior chamber intraocular lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3319a75e0b03de65e10b0bf9d84ae1ee 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. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices