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"Ruisheng" oximeter probe - Taiwan Registration bb93a95c6fa2f1692252e7917b960f23

Access comprehensive regulatory information for "Ruisheng" oximeter probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bb93a95c6fa2f1692252e7917b960f23 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, 1 companies making similar products including Ruisheng Medical Technology Co., Ltd. Zhubei Factory, and 1 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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bb93a95c6fa2f1692252e7917b960f23
Registration Details
Taiwan FDA Registration: bb93a95c6fa2f1692252e7917b960f23
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Device Details

"Ruisheng" oximeter probe
TW: โ€œ็‘ž็››โ€่ก€ๆฐงๆฟƒๅบฆ่จˆๆŽข้ ญ
Risk Class 2

Registration Details

bb93a95c6fa2f1692252e7917b960f23

DHY00500242906

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

Apr 25, 2008

Apr 25, 2028

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