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“Philips” Automated External Defibrillator - Taiwan Registration 5336308543073587dd7086d101a17326

Access comprehensive regulatory information for “Philips” Automated External Defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5336308543073587dd7086d101a17326 and manufactured by PHILIPS MEDICAL SYSTEMS. 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 use only by the Parts System Denda;;PHILIPS MEDICAL SYSTEMS, PHILIPS MEDICAL SYSTEMS, 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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5336308543073587dd7086d101a17326
Registration Details
Taiwan FDA Registration: 5336308543073587dd7086d101a17326
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Device Details

“Philips” Automated External Defibrillator
TW: “飛利浦”自動體外心臟去顫器
Risk Class 3
MD

Registration Details

5336308543073587dd7086d101a17326

Ministry of Health Medical Device Import No. 034075

DHA05603407509

Company Information

United States

Product Details

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

E Cardiovascular devices

E5310 Automated External Defibrillator

Imported from abroad

Dates and Status

Nov 09, 2020

Nov 09, 2025

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