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"Philips" patient monitor - Taiwan Registration f30c5d327e3e6b18a118895789df59e1

Access comprehensive regulatory information for "Philips" patient monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f30c5d327e3e6b18a118895789df59e1 and manufactured by PHILIPS MEDIZINSYSTEME BUBBLE GMBH;; 台灣飛利浦股份有限公司. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH, PHILIPS MEDICAL SYSTEMS, and 5 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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f30c5d327e3e6b18a118895789df59e1
Registration Details
Taiwan FDA Registration: f30c5d327e3e6b18a118895789df59e1
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Device Details

"Philips" patient monitor
TW: "飛利浦"病患監視器
Risk Class 2

Registration Details

f30c5d327e3e6b18a118895789df59e1

DHA00600800306

Company Information

Product Details

Vacuum.

E Cardiovascular Medicine Science

E.1025 Arrhythmia Detectors and Alerts

import

Dates and Status

Nov 26, 2009

Feb 09, 2029