Taiwan FDA registration ae36a4647ea97af92a8ff4ba9c5468ba
"Mikewei" vacuum powered body fluid absorption device (unsterilized)
TW: "邁柯唯"真空動力式體液吸收器具(未滅菌)
Taiwan·Risk Class 1·MAQUET GMBH·Registered Oct 05, 2011 – Oct 05, 2021CancelledRegistration details
- Analysis ID
- ae36a4647ea97af92a8ff4ba9c5468ba
- Customs Code
- DHA04401090009
Company information
- Manufacturer
- MAQUET GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Oct 05, 2011
- Expiry Date
- Oct 05, 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 "Mikewei" vacuum powered body fluid absorption device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ae36a4647ea97af92a8ff4ba9c5468ba and manufactured by MAQUET GMBH. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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