Taiwan FDA registration 856ea1e4c5500848f65d102a960dcef1
"Leishi" multiple sleep physiology recorder
TW: “磊仕”多重睡眠生理記錄儀
Taiwan·Risk Class 2·RESPIRONICS INC.·Registered Feb 20, 2012 – Feb 20, 2027ActiveRegistration details
- Analysis ID
- 856ea1e4c5500848f65d102a960dcef1
- Customs Code
- DHA00602326204
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)
- K Neuroscience
- Product Type (Level 2)
- K.1400 Brain Wave Scanner
- Import Information
- import
Dates and status
- Registration Date
- Feb 20, 2012
- Expiry Date
- Feb 20, 2027
About this record
Access comprehensive regulatory information for "Leishi" multiple sleep physiology recorder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 856ea1e4c5500848f65d102a960dcef1 and manufactured by RESPIRONICS INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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