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MEDICAL FEEDBACK TECHNOLOGIES LTD

US

Last updated May 31, 2026

What MEDICAL FEEDBACK TECHNOLOGIES LTD makes

Medical Feedback Technologies Ltd manufactures electronic cardiopulmonary resuscitation (CPR) feedback devices designed to provide real-time performance metrics for rescuers during chest compressions. The Beaty device is intended to monitor compression rate, depth, and recoil to improve the quality of CPR delivery.

The company’s portfolio is classified under FDA’s Class II regulatory category and is 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 Medical Feedback Technologies Ltd manufacture?

Medical Feedback Technologies Ltd specializes in electronic cardiopulmonary resuscitation (CPR) feedback devices. These devices are designed to give rescuers real-time feedback on chest compression performance, such as rate, depth, and recoil, to help improve the quality of CPR delivery during emergencies.

Where is Medical Feedback Technologies Ltd based?

The company is headquartered in the United States. This location influences its regulatory compliance and reporting requirements, particularly for devices marketed in the US.

Which regulatory registries list Medical Feedback Technologies Ltd’s devices?

Medical Feedback Technologies Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their Class II CPR feedback devices, ensuring transparency and traceability in the medical device supply chain.

How are Medical Feedback Technologies Ltd’s devices classified by regulatory authorities?

The company’s devices fall under the FDA’s Class II regulatory category. This classification typically means they pose moderate risk and require special controls beyond general 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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LinkedIn
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Facebook
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Email
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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
532305866

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Beaty BE8789US
FDA UDI
Class IIActive

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