“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.
Device Details
Registration Details
5336308543073587dd7086d101a17326
Ministry of Health Medical Device Import No. 034075
DHA05603407509
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
“Philips” Automated External Defibrillator
For use only by the Parts System Denda;;PHILIPS MEDICAL SYSTEMS
5574eacf59b9f71c54cdf160e73376b7
3
“Philips” Automated External Defibrillator
PHILIPS MEDICAL SYSTEMS
249a6365189b7bd8bd871a8791defb34
3

