Taiwan FDA registration c327485e9e7151ed5b5c47cb39e87e1e
"Vortex" automatic wake-up device
TW: "渦傳"自動甦醒器
Taiwan·Risk Class 2·VORTRAN MEDICAL TECHNOLOGY 1, INC.·Registered Sep 12, 2006 – Sep 12, 2016CancelledRegistration details
- Analysis ID
- c327485e9e7151ed5b5c47cb39e87e1e
- Customs Code
- DHA00601710604
Company information
- Manufacturer
- VORTRAN MEDICAL TECHNOLOGY 1, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ASIA HEALTH CARE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5925 Powered emergency breathing apparatus
- Import Information
- import
Dates and status
- Registration Date
- Sep 12, 2006
- Expiry Date
- Sep 12, 2016
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Vortex" automatic wake-up device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c327485e9e7151ed5b5c47cb39e87e1e and manufactured by VORTRAN MEDICAL TECHNOLOGY 1, INC.. The authorized representative in Taiwan is ASIA HEALTH CARE CO., LTD..
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