Taiwan FDA registration e1d65413ff551c0720ef8493117b5a35
“Vortran” GO2VENT
TW: “福全” 自動復甦器
Taiwan·Risk Class 2·MD·VORTRAN MEDICAL TECHNOLOGY 1, INC.·Registered Jun 14, 2023 – Jun 14, 2028ActiveRegistration details
- Analysis ID
- e1d65413ff551c0720ef8493117b5a35
- License Form
- Ministry of Health Medical Device Import No. 036379
- Customs Code
- DHA05603637900
Company information
- Manufacturer
- VORTRAN MEDICAL TECHNOLOGY 1, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HI-CLEARANCE INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D5925 Powered Emergency Respirator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 14, 2023
- Expiry Date
- Jun 14, 2028
About this record
Access comprehensive regulatory information for “Vortran” GO2VENT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1d65413ff551c0720ef8493117b5a35 and manufactured by VORTRAN MEDICAL TECHNOLOGY 1, INC.. The authorized representative in Taiwan is HI-CLEARANCE INC..
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