Taiwan FDA registration ec69a27581f76947958757be0f6f7687
"Red" siliceous awakening ball
TW: "雷德"矽質甦醒球
Taiwan·Risk Class 2·LAERDAL MEDICAL AS·Registered Sep 27, 2006 – Sep 27, 2021CancelledRegistration details
- Analysis ID
- ec69a27581f76947958757be0f6f7687
- Customs Code
- DHA00601732503
Company information
- Manufacturer
- LAERDAL MEDICAL AS
- Manufacturer Country
- Norway
- Authorized Representative
- Xinyi 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
- import
Dates and status
- Registration Date
- Sep 27, 2006
- Expiry Date
- Sep 27, 2021
- Cancellation Date
- Aug 28, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Red" siliceous awakening ball in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec69a27581f76947958757be0f6f7687 and manufactured by LAERDAL MEDICAL AS. The authorized representative in Taiwan is Xinyi Co., Ltd.
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