Taiwan FDA registration 5336308543073587dd7086d101a17326

“Philips” Automated External Defibrillator

TW: “飛利浦”自動體外心臟去顫器
Taiwan flagTaiwan·Risk Class 3·MD·PHILIPS MEDICAL SYSTEMS·Registered Nov 09, 2020 – Nov 09, 2025Expired
Registration details
Analysis ID
5336308543073587dd7086d101a17326
License Form
Ministry of Health Medical Device Import No. 034075
Customs Code
DHA05603407509
Company information
Manufacturer Country
United States
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
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
Nov 09, 2020
Expiry Date
Nov 09, 2025
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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 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.

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