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“Philips” Patient Monitor - Taiwan Registration 717cd2ea08aa74c79d600a4102708c47

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 717cd2ea08aa74c79d600a4102708c47 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 For spare parts system only;;PHILIPS MEDICAL SYSTEMS BOEBLINGEN GMBH, PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH;;For use only by the Parts System Denda;;For spare parts system only, 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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717cd2ea08aa74c79d600a4102708c47
Registration Details
Taiwan FDA Registration: 717cd2ea08aa74c79d600a4102708c47
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Device Details

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

Registration Details

717cd2ea08aa74c79d600a4102708c47

Ministry of Health Medical Device Import No. 032595

DHA05603259502

Company Information

China;;Germany;;Switzerland;;United States;;Costa Rica;;Poland

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

May 06, 2019

May 06, 2024