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"Io" Manual Eye Surgery Instruments (Unsterilized) - Taiwan Registration ec2add808e227fb74bd325ea196bc6e4

Access comprehensive regulatory information for "Io" Manual Eye Surgery Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec2add808e227fb74bd325ea196bc6e4 and manufactured by AMERICAN OPTISURGICAL INC.. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AMERICAN OPTISURGICAL INC., and 2 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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ec2add808e227fb74bd325ea196bc6e4
Registration Details
Taiwan FDA Registration: ec2add808e227fb74bd325ea196bc6e4
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Device Details

"Io" Manual Eye Surgery Instruments (Unsterilized)
TW: "ๆ„›ๆญ" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

ec2add808e227fb74bd325ea196bc6e4

DHA04401084402

Company Information

United States

Product Details

Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading of Medical Equipment.

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

import

Dates and Status

Sep 16, 2011

Sep 16, 2026

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