“Philips” Automated External Defibrillator
Taiwan·Risk Class 3·MD·For use only by the Parts System Denda;;PHILIPS MEDICAL SYSTEMS·Registered Sep 02, 2020 – Sep 02, 2025Expired- Analysis ID
- 5574eacf59b9f71c54cdf160e73376b7
- License Form
- Ministry of Health Medical Device Import No. 033933
- Customs Code
- DHA05603393301
- Manufacturer Country
- United States;;Austria
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- 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
- Registration Date
- Sep 02, 2020
- Expiry Date
- Sep 02, 2025
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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 5574eacf59b9f71c54cdf160e73376b7 and manufactured by For use only by the Parts System Denda;;PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including 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.