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"Singular" pathology monitor - Taiwan Registration e85ef578a7f3a1c7e9fd2a8b802a1a53

Access comprehensive regulatory information for "Singular" pathology monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e85ef578a7f3a1c7e9fd2a8b802a1a53 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 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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e85ef578a7f3a1c7e9fd2a8b802a1a53
Registration Details
Taiwan FDA Registration: e85ef578a7f3a1c7e9fd2a8b802a1a53
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Device Details

"Singular" pathology monitor
TW: "ๅฅ‡็•ฐ" ็—…็†็›ฃ่ฆ–ๅ™จ
Risk Class 2
Cancelled

Registration Details

e85ef578a7f3a1c7e9fd2a8b802a1a53

DHA00601385400

Company Information

Finland

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Dec 29, 2005

Dec 29, 2015

Apr 25, 2018

Cancellation Information

Logged out

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