Taiwan FDA registration 37aa58ed38c7b6ee53b6d8eff133fa01
"Leishi" Dream Nose Mask
TW: “磊仕” 助夢鼻面罩
Taiwan·Risk Class 2·Philips de Costa Rica S.R.L.;; RESPIRONICS INC.·Registered Aug 30, 2023 – Aug 30, 2028ActiveRegistration details
- Analysis ID
- 37aa58ed38c7b6ee53b6d8eff133fa01
- Customs Code
- DHA05603658901
Company information
- Manufacturer
- Philips de Costa Rica S.R.L.;; RESPIRONICS INC.
- Manufacturer Country
- Costa Rica;;United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5905 Non-continuous respirators
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Aug 30, 2023
- Expiry Date
- Aug 30, 2028
About this record
Access comprehensive regulatory information for "Leishi" Dream Nose Mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37aa58ed38c7b6ee53b6d8eff133fa01 and manufactured by Philips de Costa Rica S.R.L.;; RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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