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Sign in to claim this brandWhat NATUS MANUFACTURING LIMITED makes
Natus Manufacturing Limited produces single-use electromyographic needle electrodes and analytical scalp electrodes, as well as electromyographs and neurophysiologic monitoring systems. These devices are designed for clinical use in electromyography (EMG) and neurophysiologic assessments, including muscle and nerve function testing. The portfolio includes systems like Keypoint and Leadpoint, which support diagnostic procedures in neurology and physical medicine.
The company’s devices are classified as Class II under regulatory frameworks, with products listed in the FDA’s Unique Device Identifier (UDI) database. These systems are intended for use in medical settings where precise monitoring and diagnostic capabilities are required. 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 Natus Manufacturing Limited produce?
Natus Manufacturing Limited specializes in devices used for electromyography (EMG) and neurophysiologic monitoring. Their portfolio includes single-use electromyographic needle electrodes and analytical scalp electrodes, as well as electromyographs and neurophysiologic monitoring systems. These devices are designed for clinical use in assessing muscle and nerve function, supporting diagnostic procedures in neurology and physical medicine.
Where is Natus Manufacturing Limited based?
Natus Manufacturing Limited is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites may vary.
Which regulatory registries list devices manufactured by Natus Manufacturing Limited?
Devices produced by Natus Manufacturing Limited are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and identification of medical devices authorized for use in the United States.
How are the devices made by Natus Manufacturing Limited classified under regulatory standards?
The devices manufactured by Natus Manufacturing Limited fall under Class II classification in regulatory frameworks. This classification typically applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as those used in EMG and neurophysiologic monitoring.
What are some examples of devices produced by Natus Manufacturing Limited?
Natus Manufacturing Limited produces devices under brands like Keypoint and Leadpoint, which include electromyographs and neurophysiologic monitoring systems. These systems are designed for clinical use in diagnosing and evaluating muscle and nerve function, supporting specialized medical assessments.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 896421240
Catalogue (67)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Grass | F-E2-12 | FDA UDI | Class II | Active |
| Grass | F-E2-24 | FDA UDI | Class II | Active |
| Grass | EC2 | FDA UDI | Class II | Unknown |
| Keypoint | 9033S0601 | FDA UDI | Class II | Active |
| Keypoint | 9033S0731 | FDA UDI | Class II | Active |
| Grass | F-E2-48 | FDA UDI | Class II | Active |
| Natus | 9013S0032 | FDA UDI | Class II | Active |
| Dantec | 9013S0032 | FDA UDI | Class II | Active |
| Keypoint | 9033S0581 | FDA UDI | Class II | Active |
| Keypoint | 9013C0402 | FDA UDI | Class II | Active |
| Grass | F-E2-72 | FDA UDI | Class II | Active |
| Grass | F-E2-30 | FDA UDI | Class II | Active |
| Keypoint | 9031S2308 | FDA UDI | Class II | Active |
| Keypoint | 9033S0721 | FDA UDI | Class II | Active |
| Leadpoint | 9031E0752 | FDA UDI | Class II | Active |
| Leadpoint | 9033A0821AA | FDA UDI | Class II | Active |
| Leadpoint | 9033A0811AA | FDA UDI | Class II | Active |
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