“Philips” Automated External Defibrillator - Taiwan Registration 5574eacf59b9f71c54cdf160e73376b7
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 5574eacf59b9f71c54cdf160e73376b7 and manufactured by For use only by the Parts System Denda;;PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including 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.
Device Details
Registration Details
5574eacf59b9f71c54cdf160e73376b7
Ministry of Health Medical Device Import No. 033933
DHA05603393301
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
Sep 02, 2020
Sep 02, 2025

