Taiwan FDA registration 06b30f40552e34ce7be4790f81e6eef0
"Leishi" helps dream full mask
TW: “磊仕”助夢全面罩
Taiwan·Risk Class 2·Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.·Registered Jan 14, 2019 – Jan 14, 2029ActiveRegistration details
- Analysis ID
- 06b30f40552e34ce7be4790f81e6eef0
- Customs Code
- DHA09200097205
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
- Jan 14, 2019
- Expiry Date
- Jan 14, 2029
About this record
Access comprehensive regulatory information for "Leishi" helps dream full mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06b30f40552e34ce7be4790f81e6eef0 and manufactured by Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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