Home › BELMONT INSTRUMENT CORPORATION › Cerebralogik aEEG
Cerebralogik aEEG
BELMONT INSTRUMENT CORPORATION · Model Kit (CC PRO) · UDI-DI 07290102932405
10
510(k) clearances
4
Adverse events
3
Recalls
13
Facilities
Description
Electroencephalograph kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-07 | Natus Neurology DBA Excel Tech., Ltd. (XLTEK) | Electrode placement labels on the Digital Acquisition Box (DAB) were applied backwards. This may ultimately lead to misdiagnosis of seizure location in neonates monitored with this |
| 2023-02-20 | Moberg Research, Inc. | Battery leakage can cause corrosion to the metal enclosure near the electrical interface. Prolonged contact to corrosive materials could cause injury to skin. DOC |
| 2020-03-05 | Natus Neurology DBA Excel Tech., Ltd. (XLTEK) | The OBM system functional test (impedance and noise) was not carried out on the affected items prior to release to the customer. The manufacturer cannot attest to the system functi |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
