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“Philips” Patient Monitor - Taiwan Registration b8f768b788031727cccb54007ecbb171

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 b8f768b788031727cccb54007ecbb171 and manufactured by PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only, For spare parts system only;;PHILIPS MEDICAL SYSTEMS BOEBLINGEN GMBH, and 2 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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b8f768b788031727cccb54007ecbb171
Registration Details
Taiwan FDA Registration: b8f768b788031727cccb54007ecbb171
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Device Details

“Philips” Patient Monitor
TW: “飛利浦”病患監視器
Risk Class 2
MD

Registration Details

b8f768b788031727cccb54007ecbb171

Ministry of Health Medical Device Import No. 033960

DHA05603396001

Company Information

Product Details

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

E Cardiovascular devices

E1025 Arrhythmia detector and alert

Imported from abroad

Dates and Status

Sep 22, 2020

Sep 22, 2025