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"Meidus" IOL guide (sterilization) - Taiwan Registration d95db9c0ad684ce0088c875448e20448

Access comprehensive regulatory information for "Meidus" IOL 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 d95db9c0ad684ce0088c875448e20448 and manufactured by ROBUTEC AG;; MEDICEL AG. The authorized representative in Taiwan is CONEYE CO., LTD.

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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d95db9c0ad684ce0088c875448e20448
Registration Details
Taiwan FDA Registration: d95db9c0ad684ce0088c875448e20448
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Device Details

"Meidus" IOL guide (sterilization)
TW: "็พŽๅพทๆ€" ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ(ๆป…่Œ)
Risk Class 1

Registration Details

d95db9c0ad684ce0088c875448e20448

DHA09402301908

Company Information

Switzerland

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

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jan 18, 2023

Jan 18, 2028