Taiwan FDA registration f5117fcbd98dcbe79b97fdf19ccc8d57
“ResMed” AirCurve 10 VAuto Positive Airway Pressure Device
TW: “瑞思邁”艾克舒氣道正壓呼吸器
Taiwan·Risk Class 2·MD·ResMed Pty Ltd·Registered Apr 09, 2019 – Apr 09, 2024ExpiredRegistration details
- Analysis ID
- f5117fcbd98dcbe79b97fdf19ccc8d57
- License Form
- Ministry of Health Medical Device Import No. 032558
- Customs Code
- DHA05603255806
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)
- D5905 Discontinuous respirators
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 09, 2019
- Expiry Date
- Apr 09, 2024
About this record
Access comprehensive regulatory information for “ResMed” AirCurve 10 VAuto 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 f5117fcbd98dcbe79b97fdf19ccc8d57 and manufactured by ResMed Pty Ltd. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..
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