Taiwan FDA registration 2028f60e4cd20b23f5a19b7f15083a69
"Drow" Aidi defibrillator
TW: “卓爾”艾易帝除顫器
Taiwan·Risk Class 2·ZOLL MEDICAL CORPORATION·Registered Oct 01, 2008 – Oct 01, 2013CancelledRegistration details
- Analysis ID
- 2028f60e4cd20b23f5a19b7f15083a69
- Customs Code
- DHA00601923703
Company information
- Manufacturer
- ZOLL MEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- WISDOM UNION ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.5300 DC type departer (with shock board)
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2008
- Expiry Date
- Oct 01, 2013
- Cancellation Date
- Apr 09, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Drow" Aidi defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2028f60e4cd20b23f5a19b7f15083a69 and manufactured by ZOLL MEDICAL CORPORATION. The authorized representative in Taiwan is WISDOM UNION ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices