“Philips” Automated External Defibrillator
- Analysis ID
- 249a6365189b7bd8bd871a8791defb34
- License Form
- Ministry of Health Medical Device Import No. 026707
- Customs Code
- DHA05602670701
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5310 Automated External Defibrillator
- Import Information
- Imported from abroad
- Registration Date
- Dec 18, 2014
- Expiry Date
- Dec 18, 2019
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 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.