Taiwan FDA registration 9992700e4e98798b728e3007a4c7f798
"Ambu" Oxygen mask (Non-Sterile)
TW: "安普" 氧氣面罩 (未滅菌)
Taiwan·Risk Class 1·MD·AMBU A/S·Registered Aug 31, 2018 – Aug 31, 2023CancelledRegistration details
- Analysis ID
- 9992700e4e98798b728e3007a4c7f798
- License Form
- Ministry of Health Medical Device Import No. 019560
- Customs Code
- DHA09401956000
Company information
- Manufacturer
- AMBU A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- BOYANG MEDICAL TECHNOLOGY CO., LTD
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5580 oxygen mask
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 31, 2018
- Expiry Date
- Aug 31, 2023
- Cancellation Date
- Jan 10, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Ambu" Oxygen mask (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9992700e4e98798b728e3007a4c7f798 and manufactured by AMBU A/S. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY 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