Taiwan FDA registration 4fb47e24a85a0aea2bcd83553d572772
“ResMed” AirMini system
TW: “瑞思邁”亞米正壓呼吸器
Taiwan·Risk Class 2·MD·ResMed Pty Ltd·Registered Jan 02, 2018 – Jan 02, 2028ActiveRegistration details
- Analysis ID
- 4fb47e24a85a0aea2bcd83553d572772
- License Form
- Ministry of Health Medical Device Import No. 030639
- Customs Code
- DHA05603063909
Company information
- Manufacturer
- ResMed Pty Ltd
- Manufacturer Country
- Australia
- Authorized Representative
- RESMED TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5895 Continuous breathing apparatus and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 02, 2018
- Expiry Date
- Jan 02, 2028
About this record
Access comprehensive regulatory information for “ResMed” AirMini system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4fb47e24a85a0aea2bcd83553d572772 and manufactured by ResMed Pty Ltd. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..
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