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"Ruisheng" plug-in oximeter - Taiwan Registration 7851109860b47322cb0ccb679c6b0060

Access comprehensive regulatory information for "Ruisheng" plug-in oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7851109860b47322cb0ccb679c6b0060 and manufactured by Ruisheng Medical Technology Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is ROSSMAX INNOTEK CORP..

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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7851109860b47322cb0ccb679c6b0060
Registration Details
Taiwan FDA Registration: 7851109860b47322cb0ccb679c6b0060
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Device Details

"Ruisheng" plug-in oximeter
TW: โ€œ็‘ž็››โ€ๆ’้›ปๅผ่ก€ๆฐงๆฟƒๅบฆ่จˆ
Risk Class 2

Registration Details

7851109860b47322cb0ccb679c6b0060

DHY00500323906

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.2700.

Domestic

Dates and Status

May 23, 2011

May 23, 2026