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Temperature Sensor (NB-TMP)

Mind Media Europe B.V. · Model 1.0 · UDI-DI 08719481550080

HCC
10
510(k) clearances
59
Adverse events (1 deaths)
4
Recalls
108
Facilities

Description

NB-TMP: The temperature sensor provides a signal that corresponds with (variations in) peripheral skin temperature when connected to a NeXus signal acquisition device. The sensor shall be placed on intact skin to provide a signal that is influenced by cutaneous blood flow. The sensor is not intended to determine directly or indirectly a measure of core body temperature and to be used for vital monitoring purposes. The device is designed for medical use, not restricted to a specific medical indication, for acquisition of physiological signals. The device is intended to be used by, or under supervision of, a health professional within a clinical environment.

Recalls

DateFirmReason
2023-12-11RONAN MEDICAL LLCNeurofeedback systems removed due to missing design and development documentation and devices may not perform as intended.
2017-07-07Ondamed IncThe firm was marketing the Ondamed System in the US without marketing clearance. As a corrective action, the firm revised its device design to comply with regulations. The firm has
2015-10-01Powers Medical Devices, LLCPAL unit has undergone significant technological changes since the previous 510(k) and labeling is not consistent with the cleared indications of the 510(k).
2012-11-15EEG InfoEEG Info, Inc. is recalling the EEG Neuroamp device because they have identified a potential risk associated with the mislabeling of certain devices.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.