Taiwan FDA registration 6b97a6e5c59053f77b79d4b02f1e372b
“ResMed” Positive Airway Pressure Device, bi-level
TW: “瑞思邁”氣道正壓呼吸輔助器
Taiwan·Risk Class 2·MD·ResMed Pty Ltd.·Registered May 06, 2015 – May 06, 2025ExpiredRegistration details
- Analysis ID
- 6b97a6e5c59053f77b79d4b02f1e372b
- License Form
- Ministry of Health Medical Device Import No. 027285
- Customs Code
- DHA05602728503
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
- May 06, 2015
- Expiry Date
- May 06, 2025
About this record
Access comprehensive regulatory information for “ResMed” Positive Airway Pressure Device, bi-level in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b97a6e5c59053f77b79d4b02f1e372b and manufactured by ResMed Pty Ltd.. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..
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