“Philips” Automated External Defibrillator - Taiwan Registration 249a6365189b7bd8bd871a8791defb34
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 249a6365189b7bd8bd871a8791defb34 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 PHILIPS MEDICAL SYSTEMS, For use only by the Parts System Denda;;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
249a6365189b7bd8bd871a8791defb34
Ministry of Health Medical Device Import No. 026707
DHA05602670701
Product Details
E Cardiovascular devices
E5310 Automated External Defibrillator
Imported from abroad
Dates and Status
Dec 18, 2014
Dec 18, 2019
Jul 15, 2022
Cancellation Information
Logged out
未展延而逾期者
“Philips” Automated External Defibrillator
PHILIPS MEDICAL SYSTEMS
5336308543073587dd7086d101a17326
3
“Philips” Automated External Defibrillator
For use only by the Parts System Denda;;PHILIPS MEDICAL SYSTEMS
5574eacf59b9f71c54cdf160e73376b7
3

