Taiwan FDA registration 6c472e8fba4b4a75a7e0c21fe6a0e7ae
“Nox”Sleep Physiological Signals Recording System
TW: “諾克斯”睡眠生理訊號記錄系統
Taiwan·Risk Class 2·MD·Nox Medical ehf.·Registered Mar 03, 2023 – Mar 03, 2028ActiveRegistration details
- Analysis ID
- 6c472e8fba4b4a75a7e0c21fe6a0e7ae
- License Form
- Ministry of Health Medical Device Import No. 036319
- Customs Code
- DHA05603631908
Company information
- Manufacturer
- Nox Medical ehf.
- Manufacturer Country
- Iceland
- Authorized Representative
- CHANJOU CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D2375 Respiratory rate monitor
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 03, 2023
- Expiry Date
- Mar 03, 2028
About this record
Access comprehensive regulatory information for “Nox”Sleep Physiological Signals Recording System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6c472e8fba4b4a75a7e0c21fe6a0e7ae and manufactured by Nox Medical ehf.. The authorized representative in Taiwan is CHANJOU CO., LTD..
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