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Sign in to claim this brandSEER MEDICAL HOLDINGS LIMITED
US
Last updated May 31, 2026
What SEER MEDICAL HOLDINGS LIMITED makes
Seer Medical Holdings Limited manufactures electroencephalograph (EEG) devices, including the Seer Home system designed for monitoring brain activity in home or clinical settings. These devices are intended for recording electrical activity in the brain to aid in the diagnosis and management of neurological conditions.
The company’s EEG devices fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Seer Medical Holdings Limited manufacture?
Seer Medical Holdings Limited specializes in electroencephalograph (EEG) devices. These devices are designed to record electrical activity in the brain, helping healthcare professionals diagnose and monitor neurological conditions. The company’s focus is on EEG technology, which is essential for assessing brain function in both clinical and home settings.
Where is Seer Medical Holdings Limited based?
Seer Medical Holdings Limited is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework, as it operates under U.S. medical device regulations, including those enforced by the FDA.
Which regulatory registries or databases list Seer Medical Holdings Limited’s devices?
Seer Medical Holdings Limited’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.
How are Seer Medical Holdings Limited’s devices classified by regulatory authorities?
Seer Medical Holdings Limited’s EEG devices fall under FDA Class II classification. This classification is assigned based on the level of risk associated with the device. Class II devices generally require special controls in addition to general controls to ensure their safety and effectiveness, reflecting the importance of EEG monitoring in neurological diagnostics.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- seermedical.com
- —
- —
- [email protected]
- Phone
- (866) 288-5045
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 744473197
Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Seer Home | Seer App: Epilepsy Management | FDA UDI | Class II | Unknown |
| Seer Home | SM-01-9008 | FDA UDI | Class I | Unknown |
| Seer Home | Seer Cloud | FDA UDI | Class II | Active |
| Seer Home | SM-03-8001-INT | FDA UDI | Class II | Unknown |
| Seer Home | SM-01-9005 | FDA UDI | Class I | Unknown |
| Seer Home | SM-07-8001 | FDA UDI | Class II | Unknown |
| Seer Home | SM-01-9008 | FDA UDI | Class I | Unknown |
| Seer Home | SM-07-8001 | FDA UDI | Class II | Unknown |
| Seer Home | Monitoring Portal | FDA UDI | Class II | Unknown |
| Seer Home | Seer App: Epilepsy Management | FDA UDI | Class II | Unknown |
| Seer Home | SM-01-9005 | FDA UDI | Class I | Unknown |
| Seer Home | SM-01-8001 | FDA UDI | Class II | Unknown |
| Seer Home | Seer Cloud | FDA UDI | Class II | Unknown |
| Seer Home | SM-03-8001-INT | FDA UDI | Class II | Unknown |
| Seer Home | SM-01-8001 | FDA UDI | Class II | Unknown |
| Seer Home | Monitoring Portal | FDA UDI | Class II | Unknown |
| Seer Home | SM-01-9003-US | FDA UDI | Class I | Unknown |
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