Taiwan FDA registration c7f890df48bfa0909edf2ef9c428851b
"Flex" non-contact respiratory rate monitoring system
TW: "醫倍思"非接觸式呼吸頻率監測系統
Taiwan·Risk Class 2·WISTRON MEDICAL TECHNOLOGY CORPORATION·Registered Jul 23, 2023 – Jul 23, 2028ActiveRegistration details
- Analysis ID
- c7f890df48bfa0909edf2ef9c428851b
Company information
- Manufacturer
- WISTRON MEDICAL TECHNOLOGY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WISTRON MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology; E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2910 Receivers for Physiological Signal Transmission by Radio Waves;; D.2375 Respiratory Rate Monitor
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 23, 2023
- Expiry Date
- Jul 23, 2028
About this record
Access comprehensive regulatory information for "Flex" non-contact respiratory rate monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c7f890df48bfa0909edf2ef9c428851b and manufactured by WISTRON MEDICAL TECHNOLOGY CORPORATION. The authorized representative in Taiwan is WISTRON MEDICAL TECHNOLOGY CORPORATION.
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