Taiwan FDA registration 249a6365189b7bd8bd871a8791defb34

“Philips” Automated External Defibrillator

TW: “飛利浦”自動體外心臟去纖維顫動器
Taiwan flagTaiwan·Risk Class 3·MD·PHILIPS MEDICAL SYSTEMS·Registered Dec 18, 2014 – Dec 18, 2019Cancelled
Registration details
Analysis ID
249a6365189b7bd8bd871a8791defb34
License Form
Ministry of Health Medical Device Import No. 026707
Customs Code
DHA05602670701
Company information
Manufacturer Country
United States
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E5310 Automated External Defibrillator
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 18, 2014
Expiry Date
Dec 18, 2019
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

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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