Manual/DEA Defibrillator Monitor YR07033

The manual/DEA defibrillator monitor YR07033 is a biphasic device designed to support emergency cardiac care in hospitals, clinics, ambulances, and intensive care units. It combines two defibrillation modes —manual and DEA (automated external defibrillator)— with ECG monitoring, allowing healthcare personnel to assess the heart rhythm and act according to the applicable clinical protocol.

Its high-resolution 7-inch display facilitates the visualization of information during care. The device has a scanning speed of 25 mm/s, a built-in battery, and a SpO₂ module. Its dimensions of 328 × 248 × 281 mm and a weight of 2 kg, according to the technical data sheet, allow for integration in clinical spaces and transport between care areas.

The biphasic defibrillation technology of the YR07033 and its manual and DEA modes make it a suitable option for centers that require a versatile defibrillator monitor. Before making a purchase, it is advisable to confirm which accessories are included in the proposed configuration and verify compatibility with the protocols and requirements of the healthcare center.

Market Price

The price of a biphasic defibrillator monitor with a 7-inch display may vary depending on the brand, monitoring configuration, included accessories, warranty, technical support, and country of purchase. As a reference, some similar devices are found in the range of US$930 to US$1030. This figure is indicative and does not represent an offer for the model YR07033.

Frequently Asked Questions

Does the YR07033 operate in manual and DEA mode?

Yes. The product sheet indicates two defibrillation modes: manual and DEA. The appropriate mode should be selected based on the patient's condition, the operator's training, and the established care protocol.

Does the device allow ECG monitoring?

Yes. Among the specified functions is ECG monitoring. The sheet also indicates that it includes a SpO₂ module.

What is the size of the display?

It has a high-resolution 7-inch display, equivalent to approximately 17.7 cm diagonally.

What are the dimensions and weight of the device?

The indicated dimensions are 328 × 248 × 281 mm and the specified weight is 2 kg. It is recommended to confirm the transport weight and packaging dimensions when planning the shipment.

Does it include all necessary accessories for use?

The provided information does not detail the contents of the configuration. Before purchasing, confirm with the supplier whether it includes the battery, cables, electrodes, SpO₂ sensors, paddles, or other necessary accessories.

Advantages and Aspects to Confirm

Among its advantages are the combination of manual and DEA defibrillation, biphasic technology, the 7-inch display, and the indicated ECG and SpO₂ monitoring functions. The specified size and weight may also facilitate its transport between care spaces.

The available sheet does not specify parameters such as battery life, energy ranges, protection against liquids or dust, record printing, external pacing, or included accessories. This information may be important for comparing models and planning their use. It is recommended to request this information before purchase and confirm that the device meets the center's needs.

Product Use in the Field

In a cardiac emergency, healthcare personnel can use the YR07033 to monitor the ECG and, based on clinical assessment, apply the manual or DEA mode. The display allows for consulting patient information during care, while the SpO₂ module can contribute to monitoring oxygenation when used with the compatible sensor.

The device can be integrated into emergency areas, procedure rooms, critical care units, and ambulances, provided that the configuration, accessories, and transport conditions are appropriate. It must be used by qualified personnel, following the manufacturer's instructions and local clinical protocols.

Recommendations

Before operating the defibrillator monitor, review the manual, check the accessories, and verify the battery status. Establish a periodic inspection program and confirm that consumables and components are available and compatible with the device.

Train the personnel who will use it and perform the checks recommended by the manufacturer. If it will be used in ambulances or during transfers, confirm the transport and securing conditions of the device. It is also recommended to request from the supplier information about the warranty, technical support, maintenance, and the exact contents of the offer.