Taiwan FDA registration 2de7544a38098903b223793b2a262da7
"Leishi" Dream Booster Nasal Mask
TW: “磊仕”助夢鼻面罩
Taiwan·Risk Class 2·Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.·Registered Mar 16, 2016 – Mar 16, 2026ExpiredRegistration details
- Analysis ID
- 2de7544a38098903b223793b2a262da7
- Customs Code
- DHA09200074902
Company information
- Manufacturer Country
- United States;;China
- 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.5905 Non-continuous respirators
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 16, 2016
- Expiry Date
- Mar 16, 2026
About this record
Access comprehensive regulatory information for "Leishi" Dream Booster Nasal Mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2de7544a38098903b223793b2a262da7 and manufactured by Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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