Taiwan FDA registration 751ce8d6ac878912f977b7fa94886ec4
"Amber" Mark Mitri Awakener
TW: “安寶”馬克米特力甦醒器
Taiwan·Risk Class 2·AMBU A/S;; AMBU LTD.·Registered Oct 04, 2011 – Oct 04, 2016CancelledRegistration details
- Analysis ID
- 751ce8d6ac878912f977b7fa94886ec4
- Customs Code
- DHA04200038803
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
- Oct 04, 2011
- Expiry Date
- Oct 04, 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 Mitri Awakener in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 751ce8d6ac878912f977b7fa94886ec4 and manufactured by AMBU A/S;; AMBU LTD.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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