Taiwan FDA registration 3ba796dcf74bd3e03a9b7bd2162121a4
“ResMed” Quattro Air Non-Vented Full Face mask
TW: “瑞思邁”卓越無通氣孔面罩
Taiwan·Risk Class 2·MD·RESMED LIMITED·Registered Jan 28, 2019 – Jan 28, 2024ExpiredRegistration details
- Analysis ID
- 3ba796dcf74bd3e03a9b7bd2162121a4
- License Form
- Ministry of Health Medical Device Import No. 032091
- Customs Code
- DHA05603209100
Company information
- Manufacturer
- RESMED LIMITED
- 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
- Jan 28, 2019
- Expiry Date
- Jan 28, 2024
About this record
Access comprehensive regulatory information for “ResMed” Quattro Air Non-Vented Full Face mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3ba796dcf74bd3e03a9b7bd2162121a4 and manufactured by RESMED LIMITED. The authorized representative in Taiwan is RESMED TAIWAN CO., LTD..
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