Taiwan FDA registration 03cbf4f1d7c8d97512b51184ad49a3eb
“Ambu” SPUR II Resuscitator
TW: “安佈”思璞甦醒器
Taiwan·Risk Class 2·MD·AMBU LIMITED;;AMBU A/S·Registered Jul 22, 2019 – Jul 22, 2024ExpiredRegistration details
- Analysis ID
- 03cbf4f1d7c8d97512b51184ad49a3eb
- License Form
- Ministry of Health Medical Device Land Transport No. 001051
- Customs Code
- DHA09200105105
Company information
- Manufacturer
- AMBU LIMITED;;AMBU A/S
- Manufacturer Country
- Denmark;;China
- Authorized Representative
- HWA YI MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5915 Manual Emergency Respirator
- Import Information
- Imported from abroad; Contract manufacturing;; Made in China
Dates and status
- Registration Date
- Jul 22, 2019
- Expiry Date
- Jul 22, 2024
About this record
Access comprehensive regulatory information for “Ambu” SPUR II Resuscitator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03cbf4f1d7c8d97512b51184ad49a3eb and manufactured by AMBU LIMITED;;AMBU A/S. The authorized representative in Taiwan is HWA YI MEDICAL CO., LTD..
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