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"Noni" pulse oximetry - Taiwan Registration 2309b4a42c6fb2b62bb64f223c2fe0bc

Access comprehensive regulatory information for "Noni" pulse oximetry in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2309b4a42c6fb2b62bb64f223c2fe0bc and manufactured by NONIN MEDICAL, INC.. The authorized representative in Taiwan is AMY GRANT 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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2309b4a42c6fb2b62bb64f223c2fe0bc
Registration Details
Taiwan FDA Registration: 2309b4a42c6fb2b62bb64f223c2fe0bc
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Device Details

"Noni" pulse oximetry
TW: "่ซพๅฐผ"่„ˆๆ่ก€ๆฐง้ฃฝๅ’Œๆธฌๅฎšๅ„€
Risk Class 2
Cancelled

Registration Details

2309b4a42c6fb2b62bb64f223c2fe0bc

DHA00601697409

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

Aug 08, 2006

Aug 08, 2011

Jan 17, 2013

Cancellation Information

Logged out

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