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"Haninda" intraocular lens guide (sterilization) - Taiwan Registration cc4870c2fd03e9e25907b3aced7b7421

Access comprehensive regulatory information for "Haninda" intraocular lens guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cc4870c2fd03e9e25907b3aced7b7421 and manufactured by HANITA LENSES. The authorized representative in Taiwan is OCU-MED INC..

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.

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cc4870c2fd03e9e25907b3aced7b7421
Registration Details
Taiwan FDA Registration: cc4870c2fd03e9e25907b3aced7b7421
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Device Details

"Haninda" intraocular lens guide (sterilization)
TW: "ๆผขๅฏง้”" ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ (ๆป…่Œ)
Risk Class 1

Registration Details

cc4870c2fd03e9e25907b3aced7b7421

DHA09401516803

Company Information

Israel

Product Details

Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.

M Ophthalmology

M.4300 Artificial crystal body inducer

Input;; QMS/QSD

Dates and Status

Apr 28, 2015

Apr 28, 2025