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Sign in to claim this brandShenzhen Coreray Technology, Ltd.
US
Last updated May 23, 2026
What Shenzhen Coreray Technology, Ltd. makes
The company manufactures reusable electrocardiographic lead sets, including ECG cables and leadwires for patient monitoring, as well as reusable blood pressure cuffs and pulse oximeter probes for SpO2 monitoring. Their portfolio includes reusable SpO2 sensors and extension cables designed for continuous vital sign tracking.
These devices are classified as Class II under regulatory frameworks and are listed in the FDA’s 510(k) and UDI registries. The company 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 Shenzhen Coreray Technology, Ltd. manufacture?
Shenzhen Coreray Technology, Ltd. specializes in reusable medical devices primarily used for patient monitoring. Their portfolio includes electrocardiographic (ECG) lead sets such as reusable ECG cables and leadwires, reusable blood pressure cuffs, and reusable pulse oximeter probes (SpO2 sensors). These devices are designed for continuous tracking of vital signs like heart rate, blood pressure, and oxygen saturation.
Where is Shenzhen Coreray Technology, Ltd. based?
The company is based in the United States. While their name suggests an origin in Shenzhen, their operational headquarters and manufacturing presence are located within the US.
Which regulatory registries list Shenzhen Coreray Technology, Ltd.’s devices?
The company’s devices are listed in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identifier (UDI) database. These registries track devices that have undergone the necessary regulatory pathways for market authorization in the US.
How are Shenzhen Coreray Technology, Ltd.’s devices classified under regulatory frameworks?
Shenzhen Coreray Technology, Ltd.’s devices fall under Class II classification in regulatory frameworks. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as reusable monitoring leads and sensors.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| coreray ECG cable | CR005-7302 | FDA UDI | Class II | Active |
| coreray ECG cable | CR005-0401 | FDA UDI | Class II | Active |
| Aile | CR009-R-PU-005 | FDA UDI | Class II | Active |
| coreray ECG cable | CR005-7301 | FDA UDI | Class II | Active |
| coreray reusable SpO2 sensor | CR001-3106A | FDA UDI | Class II | Active |
| coreray EKG cable | CR007-5502 | FDA UDI | Class II | Active |
| ECG Cable/Leadwires | K172797 | FDA 510(k) | Class II | Active |
| Patient Monitoring Cable (SpO2 Extension Cable) | K192404 | FDA 510(k) | Class II | Active |
| Reusable & Disposable SpO2 Sensors | K173368 | FDA 510(k) | Class II | Active |
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