Taiwan FDA registration 4f5f641f1524f0b2a46d51df82c3cec7
"Ambo" Oufu awakener
TW: “安寶”歐輔甦醒器
Taiwan·Risk Class 2·AMBU A/S;; AMBU LTD.·Registered Jul 16, 2012 – Jul 16, 2017CancelledRegistration details
- Analysis ID
- 4f5f641f1524f0b2a46d51df82c3cec7
- Customs Code
- DHA04200043400
Company information
- Manufacturer
- AMBU A/S;; AMBU LTD.
- Manufacturer Country
- Denmark;;China
- Authorized Representative
- CHINA SPRING TRADING 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
Dates and status
- Registration Date
- Jul 16, 2012
- Expiry Date
- Jul 16, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ambo" Oufu awakener in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4f5f641f1524f0b2a46d51df82c3cec7 and manufactured by AMBU A/S;; AMBU LTD.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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