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Essilor Forerunner (Unsterilized) - Taiwan Registration fd20d4926fd48f092525d0acad9eb319

Access comprehensive regulatory information for Essilor Forerunner (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd20d4926fd48f092525d0acad9eb319 and manufactured by VISIONIX LTD;; ESSILOR INTERNATIONAL. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VISIONIX LTD;; ESSILOR INTERNATIONAL, 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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fd20d4926fd48f092525d0acad9eb319
Registration Details
Taiwan FDA Registration: fd20d4926fd48f092525d0acad9eb319
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Device Details

Essilor Forerunner (Unsterilized)
TW: "ไพ่ฆ–่ทฏ" ๅ‰ๅฐŽๆณขๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

fd20d4926fd48f092525d0acad9eb319

DHA08401769501

Company Information

France;;Israel

Product Details

Limited to the first level identification scope of the "Automatic Ophthalmic Refractive Machine (M.1760)" of the Measures for the Classification and Grading of Medical Equipment.

M Ophthalmology

M.1760 Automatic Ophthalmic Optical Machine

่ผธๅ…ฅ;; ๅง”่จ—่ฃฝ้€ ;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2025

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