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"Strange" 麻醉監視器 - Taiwan Registration 8c08c2685a3d05714a9dc6730f36b17f

Access comprehensive regulatory information for "Strange" 麻醉監視器 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8c08c2685a3d05714a9dc6730f36b17f 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 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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8c08c2685a3d05714a9dc6730f36b17f
Registration Details
Taiwan FDA Registration: 8c08c2685a3d05714a9dc6730f36b17f
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Device Details

"Strange" 麻醉監視器
TW: "奇異" 麻醉監視器
Risk Class 2
Cancelled

Registration Details

8c08c2685a3d05714a9dc6730f36b17f

DHA00601279005

Company Information

Finland

Product Details

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

E Cardiovascular Medicine Science

E.1025 Arrhythmia Detectors and Alerts

import

Dates and Status

Oct 26, 2005

Oct 26, 2015

Apr 25, 2018

Cancellation Information

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