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“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.

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249a6365189b7bd8bd871a8791defb34
Registration Details
Taiwan FDA Registration: 249a6365189b7bd8bd871a8791defb34
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Device Details

“Philips” Automated External Defibrillator
TW: “飛利浦”自動體外心臟去纖維顫動器
Risk Class 3
MD
Cancelled

Registration Details

249a6365189b7bd8bd871a8791defb34

Ministry of Health Medical Device Import No. 026707

DHA05602670701

Company Information

United States

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

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