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"Philips" patient monitor - Taiwan Registration f537bf065411512c5d13f8bf8e006d46

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 f537bf065411512c5d13f8bf8e006d46 and manufactured by PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including PHILIPS MEDICAL SYSTEMS, PHILIPS MEDIZINSYSTEME BÖBLINGEN GMBH, 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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f537bf065411512c5d13f8bf8e006d46
Registration Details
Taiwan FDA Registration: f537bf065411512c5d13f8bf8e006d46
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Device Details

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

Registration Details

f537bf065411512c5d13f8bf8e006d46

DHA00602265801

Company Information

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

Jul 29, 2011

Jul 29, 2026