Nox Medical
Active in EUDAMEDIcelandfrom SRN EUDAMED FDA SRN IS-MF-000000950 FEI 3007389703
- Devices
- 103
- Registrations
- EUDAMEDFDA
- FDA recalls
- 1
What Nox Medical makes
Nox Medical manufactures respiratory monitoring devices including the Nox T3s System, Nox A1S SAS kit, T3s Recorder, and various RIP belts in different sizes, along with accessories like snap-on leads and body cables.
The company's products are classified as Class I, Class II, and Class IIa medical devices and are listed in the EU's EUDAMED and FDA's 510(k) databases. Nox Medical is based in Iceland.
Catalogue
Search and filter all 103 devicesNox Abdomen Cable Ref 562010
Regimes: CE MDR Registry: EUDAMEDGUDIDNox A1® EEG Head Cable Ref 562110
Regimes: CE MDR Registry: EUDAMEDGUDIDNox RIP Belts Disposable - Large Ref 951042
Regimes: CE MDR Registry: EUDAMEDGUDID
Showing 101-103 of 103
Company details
- EUDAMED SRN
- IS-MF-000000950
- SRN (system / procedure pack)
- IS-PR-000054327
- FDA FEI number
- 3007389703
- EU VAT number
- 98087
- EUDAMED status
- Active
- EUDAMED registered name
- Nox Medical
- Registered address
- 2, Katrinartun, 105, Reykjavik, Iceland
- Website
- noxmedical.com
- [email protected]
- Phone
- 354 5707170
- PRRC contact
- Robert Magnusson
FDA recalls
FDA recall records list 1 recall initiated by Nox Medical, initiated on 2021-09-07. By recorded status: 1 terminated. The reasons filed fall into these groups: software or firmware and performance or accuracy. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 1
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2021
- 7 Sep 2021 Z-0031-2022 Class II Terminated Error in the device firmware results in the inaccurate detection of device position.