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"Ateke" Hand Ophthalmic Surgical Device (Uninverted) - Taiwan Registration d8480b278ea308efe891cdf52bfb3fdf

Access comprehensive regulatory information for "Ateke" Hand Ophthalmic Surgical Device (Uninverted) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d8480b278ea308efe891cdf52bfb3fdf and manufactured by EYE TECHNOLOGY LTD. The authorized representative in Taiwan is CRYSTALVISION 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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d8480b278ea308efe891cdf52bfb3fdf
Registration Details
Taiwan FDA Registration: d8480b278ea308efe891cdf52bfb3fdf
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Device Details

"Ateke" Hand Ophthalmic Surgical Device (Uninverted)
TW: "่‰พ็‰นๅ…‹" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d8480b278ea308efe891cdf52bfb3fdf

DHA09402349501

Company Information

United Kingdom

Product Details

It is limited to the first level of identification of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Administrative Measures for the Classification and Grading of Medical Devices.

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

Input;; QMS/QSD

Dates and Status

May 31, 2024

May 31, 2029