Taiwan FDA registration 22f22dfaa906c75ae922c54b01802b8a
ResMed AirStart Positive Airway Pressure Device
TW: 瑞思邁亞治達氣道正壓呼吸器
Taiwan·Risk Class 2·MD·ResMed Pty Ltd·Registered Dec 08, 2016 – Dec 08, 2026ActiveRegistration details
- Analysis ID
- 22f22dfaa906c75ae922c54b01802b8a
- License Form
- Ministry of Health Medical Device Import No. 029135
- Customs Code
- DHA05602913507
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
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 08, 2016
- Expiry Date
- Dec 08, 2026
About this record
Access comprehensive regulatory information for ResMed AirStart Positive Airway Pressure Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22f22dfaa906c75ae922c54b01802b8a and manufactured by ResMed Pty Ltd. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..
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