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"Singular" pathology monitor - Taiwan Registration 282d24e9ea8339c1829d73499869d01f

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 282d24e9ea8339c1829d73499869d01f and manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES. 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 FINLAND OY, 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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282d24e9ea8339c1829d73499869d01f
Registration Details
Taiwan FDA Registration: 282d24e9ea8339c1829d73499869d01f
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Device Details

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

Registration Details

282d24e9ea8339c1829d73499869d01f

DHA00601440703

Company Information

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

May 04, 2006

May 04, 2016

Apr 25, 2018

Cancellation Information

Logged out

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