Taiwan FDA registration c0f8e5bf66587f049d9e76d748f5fc78
"Ambu" Sipu awakener and its accessories
TW: “安佈”思璞甦醒器及其配件
Taiwan·Risk Class 2·AMBU LIMITED;; AMBU A/S·Registered Jul 22, 2019 – Jul 22, 2029ActiveRegistration details
- Analysis ID
- c0f8e5bf66587f049d9e76d748f5fc78
- 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 Anesthesiology
- Product Type (Level 2)
- D.5915 Hand emergency breathing apparatus
- Import Information
- Contract manufacturing;; Input;; Chinese goods
Dates and status
- Registration Date
- Jul 22, 2019
- Expiry Date
- Jul 22, 2029
About this record
Access comprehensive regulatory information for "Ambu" Sipu awakener and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c0f8e5bf66587f049d9e76d748f5fc78 and manufactured by AMBU LIMITED;; AMBU A/S. The authorized representative in Taiwan is HWA YI MEDICAL CO., LTD..
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