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"Suba" eyewash (unsterilized) - Taiwan Registration 3e8cc837532cc30ee7c3be72ca036b35

Access comprehensive regulatory information for "Suba" eyewash (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3e8cc837532cc30ee7c3be72ca036b35 and manufactured by Amedifact Co., Ltd.. The authorized representative in Taiwan is Yuancheng Xingye 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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3e8cc837532cc30ee7c3be72ca036b35
Registration Details
Taiwan FDA Registration: 3e8cc837532cc30ee7c3be72ca036b35
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Device Details

"Suba" eyewash (unsterilized)
TW: โ€œๆ–ฏๅทดโ€ๆด—็œผๅ™จ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1

Registration Details

3e8cc837532cc30ee7c3be72ca036b35

Company Information

Taiwan, Province of China

Product Details

It is limited to the first-level identification scope of the "Liquid Drug Dispenser (J.6430)" Administrative Measures for the Classification and Grading of Medical Devices.

J General hospital and personal use equipment

J.6430 ๆถฒ้ซ”่—ฅ็‰ฉ็ตฆ่—ฅๅ™จ

Contract manufacturing;; Domestic

Dates and Status

Jun 28, 2010

Jun 28, 2025