Taiwan FDA registration f433cf6aa915258d5db7f65fa95e4c17
"Leishi" heated humidifier
TW: “磊仕”加熱型潮濕器
Taiwan·Risk Class 2·RESPIRONICS INC.·Registered Jan 08, 2013 – Jan 08, 2028ActiveRegistration details
- Analysis ID
- f433cf6aa915258d5db7f65fa95e4c17
- Customs Code
- DHA00602438601
Company information
- Manufacturer
- RESPIRONICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5450 Vapor moisture apparatus for respirators
- Import Information
- import
Dates and status
- Registration Date
- Jan 08, 2013
- Expiry Date
- Jan 08, 2028
About this record
Access comprehensive regulatory information for "Leishi" heated humidifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f433cf6aa915258d5db7f65fa95e4c17 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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