Taiwan FDA registration 955396657e885c2b8c21d4bebe9f7d57
“RESMED”Therapeutic humidifier for home use (Non-Sterile)
TW: “瑞思邁”居家用治療潮濕器 (未滅菌)
Taiwan·Risk Class 1·MD·ResMed Pty Ltd·Registered Sep 18, 2013 – Sep 18, 2028ActiveRegistration details
- Analysis ID
- 955396657e885c2b8c21d4bebe9f7d57
- License Form
- Ministry of Health Medical Device Import No. 013439
- Customs Code
- DHA09401343901
Company information
- Manufacturer
- ResMed Pty Ltd
- Manufacturer Country
- Australia
- Authorized Representative
- RESMED TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Household Treatment Moisturizer (D.5460)".
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5460 Household Therapeutic Moisturizer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 18, 2013
- Expiry Date
- Sep 18, 2028
About this record
Access comprehensive regulatory information for “RESMED”Therapeutic humidifier for home use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 955396657e885c2b8c21d4bebe9f7d57 and manufactured by ResMed Pty Ltd. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..
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