Taiwan FDA registration f5177246461808cb6e6120032dbd21e9
"Leishi" Cerobi mask
TW: “磊仕” 賽若比面罩
Taiwan·Risk Class 2·RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.·Registered Apr 20, 2023 – Apr 20, 2028ActiveRegistration details
- Analysis ID
- f5177246461808cb6e6120032dbd21e9
- Customs Code
- DHA09200144003
Company information
- Manufacturer Country
- United States;;China
- 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
- Chinese goods;; input
Dates and status
- Registration Date
- Apr 20, 2023
- Expiry Date
- Apr 20, 2028
About this record
Access comprehensive regulatory information for "Leishi" Cerobi mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5177246461808cb6e6120032dbd21e9 and manufactured by RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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