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"Singular" oximetry - Taiwan Registration 8aaf0e3460604adc38d0d04829297a60

Access comprehensive regulatory information for "Singular" oximetry in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8aaf0e3460604adc38d0d04829297a60 and manufactured by GE HEALTHCARE FINLAND OY. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GE HEALTHCARE-CRITIKON DE MEXICO S. DE R.L. DE C.V.; GE Medical Systems Information Technologies, 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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8aaf0e3460604adc38d0d04829297a60
Registration Details
Taiwan FDA Registration: 8aaf0e3460604adc38d0d04829297a60
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Device Details

"Singular" oximetry
TW: "ๅฅ‡็•ฐ" ่ก€ๆฐง้ฃฝๅ’Œๆธฌๅฎšๅ„€
Risk Class 2
Cancelled

Registration Details

8aaf0e3460604adc38d0d04829297a60

DHA00601355207

Company Information

Finland

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Nov 11, 2005

Nov 11, 2015

Apr 25, 2018

Cancellation Information

Logged out

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