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"Io" Manual Eye Surgery Instruments (Unsterilized)  - Taiwan Registration 6439a298fd5a7e782ed80a0a25f30162

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 6439a298fd5a7e782ed80a0a25f30162 and manufactured by AMERICAN OPTISURGICAL INC.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT 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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6439a298fd5a7e782ed80a0a25f30162
Registration Details
Taiwan FDA Registration: 6439a298fd5a7e782ed80a0a25f30162
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Device Details

"Io" Manual Eye Surgery Instruments (Unsterilized) 
TW: “愛歐”手動式眼科手術器械 (未滅菌) 
Risk Class 1
Cancelled

Registration Details

6439a298fd5a7e782ed80a0a25f30162

DHA04400976200

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".

M Ophthalmology

M.4350 手動式眼科手術器械

import

Dates and Status

Dec 30, 2010

Dec 30, 2015

Jun 25, 2018

Cancellation Information

Logged out

許可證已逾有效期