Taiwan FDA registration e53ad436fa221421e2ad02622380eb48
“ZOLL” X-Series Defibrillator
TW: “卓爾”艾克斯系列除顫系統
Taiwan·Risk Class 3·MD·For use only by the Parts System Denda;;ZOLL MEDICAL CORPORATION·Registered Aug 01, 2016 – Aug 01, 2026ActiveRegistration details
- Analysis ID
- e53ad436fa221421e2ad02622380eb48
- License Form
- Ministry of Health Medical Device Import No. 028648
- Customs Code
- DHA05602864805
Company information
- Manufacturer Country
- United States;;Mexico
- Authorized Representative
- ZOLL MEDICAL TAIWAN CO., LTD
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
- Aug 01, 2016
- Expiry Date
- Aug 01, 2026
About this record
Access comprehensive regulatory information for “ZOLL” X-Series Defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e53ad436fa221421e2ad02622380eb48 and manufactured by For use only by the Parts System Denda;;ZOLL MEDICAL CORPORATION. The authorized representative in Taiwan is ZOLL MEDICAL TAIWAN CO., LTD.
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