Taiwan FDA registration 69aeae737957bf6127a0b4c1aaeda9a8
"Amber" Mark Awakener
TW: “安寶”馬克甦醒器
Taiwan·Risk Class 2·AMBU A/S;; AMBU LTD.·Registered Sep 22, 2011 – Sep 22, 2016CancelledRegistration details
- Analysis ID
- 69aeae737957bf6127a0b4c1aaeda9a8
- Customs Code
- DHA04200038701
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
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Sep 22, 2011
- Expiry Date
- Sep 22, 2016
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Amber" Mark Awakener in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 69aeae737957bf6127a0b4c1aaeda9a8 and manufactured by AMBU A/S;; AMBU LTD.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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