Taiwan FDA registration 35993f10be86ba614ec9eab35ca452bc
“AirSep” NewLife Oxygen Concentrator
TW: “艾爾斯” 新生型氧氣濃縮機
Taiwan·Risk Class 2·MD·AIRSEP CORPORATION·Registered Sep 24, 2013 – Sep 24, 2018CancelledRegistration details
- Analysis ID
- 35993f10be86ba614ec9eab35ca452bc
- License Form
- Ministry of Health Medical Device Import No. 025245
- Customs Code
- DHA05602524507
Company information
- Manufacturer
- AIRSEP CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- TAI CHI ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5440 portable oxygen generator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 24, 2013
- Expiry Date
- Sep 24, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “AirSep” NewLife Oxygen Concentrator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 35993f10be86ba614ec9eab35ca452bc and manufactured by AIRSEP CORPORATION. The authorized representative in Taiwan is TAI CHI ENTERPRISE CO., LTD..
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