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Sign in to claim this brandM F Equipamentos Medicos Ltda Epp
US
Last updated May 27, 2026
What M F Equipamentos Medicos Ltda Epp makes
M F Equipamentos Médicos Ltda EPP manufactures electroencephalographs and polysomnographs, including multiple models of the Neurovirtual system. These devices are designed for recording and analyzing electrical activity in the brain and monitoring physiological parameters during sleep studies, respectively.
The company’s products are classified as Class II devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 M F Equipamentos Médicos Ltda EPP manufacture?
M F Equipamentos Médicos Ltda EPP specializes in electroencephalographs and polysomnographs. Electroencephalographs (such as the Neurovirtual system) record brain activity, while polysomnographs monitor multiple physiological parameters during sleep studies. These devices are used in clinical settings to diagnose neurological conditions and sleep disorders.
Where is M F Equipamentos Médicos Ltda EPP based?
The company is based in the United States. This location is relevant for regulatory compliance, as it influences the jurisdiction under which its devices may be authorized and marketed.
Which regulatory registries list M F Equipamentos Médicos Ltda EPP’s devices?
The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to verify device details and compliance.
How are M F Equipamentos Médicos Ltda EPP’s devices classified under FDA regulations?
The company’s devices, including its Neurovirtual systems, are classified as Class II under FDA regulations. This classification typically applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 904571309
Catalogue (8)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Neurovirtual | BWIII EEG Plus | FDA UDI | Class II | Active |
| Neurovirtual | BWMini EEG | FDA UDI | Class II | Active |
| Neurovirtual | BWII EEG Digital | FDA UDI | Class II | Active |
| Neurovirtual | BWMini HST | FDA UDI | Class II | Active |
| Neurovirtual | BWIII EEG | FDA UDI | Class II | Active |
| Neurovirtual | BWII PSG Digital | FDA UDI | Class II | Active |
| Neurovirtual | BWMini PSG | FDA UDI | Class II | Active |
| Neurovirtual | BWIII PSG | FDA UDI | Class II | Active |
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