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"Nonin" handheld type oximetry tester - Taiwan Registration 15c943de87e7f7348d91459207ab6b9c

Access comprehensive regulatory information for "Nonin" handheld type oximetry tester in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 15c943de87e7f7348d91459207ab6b9c and manufactured by NONIN MEDICAL, INC.. The authorized representative in Taiwan is BIOSYSTEMS INC..

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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15c943de87e7f7348d91459207ab6b9c
Registration Details
Taiwan FDA Registration: 15c943de87e7f7348d91459207ab6b9c
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Device Details

"Nonin" handheld type oximetry tester
TW: โ€œ่ซพๅฏงโ€ๆŽŒไธŠๅž‹่ก€ๆฐง้ฃฝๅ’Œๆธฌๅฎšๅ„€
Risk Class 2

Registration Details

15c943de87e7f7348d91459207ab6b9c

DHA00602050706

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.2700.

import

Dates and Status

Dec 22, 2009

Dec 22, 2029