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RBD GROUP, LLC

US

Last updated May 30, 2026

What RBD GROUP, LLC makes

RBD Group, LLC manufactures portable electronic sphygmomanometers designed for automatic inflation, intended for use on the arm or wrist. These devices are primarily used to measure blood pressure in clinical and home settings.

The company’s products fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in 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 RBD Group, LLC manufacture?

RBD Group, LLC specializes in portable electronic sphygmomanometers that automatically inflate. These devices are designed for use on either the arm or wrist and are intended for measuring blood pressure in both clinical and home environments. Their focus is on blood pressure monitoring solutions.

Where is RBD Group, LLC based?

RBD Group, LLC is headquartered in the United States. The company’s location is relevant for regulatory compliance and distribution, particularly for devices intended for the US market.

Which regulatory registries or databases list RBD Group, LLC’s devices?

RBD Group, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices for regulatory, safety, and market surveillance purposes, ensuring traceability and compliance.

How are RBD Group, LLC’s devices classified by regulatory authorities?

RBD Group, LLC’s devices fall under FDA Class II regulation. This classification typically applies to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as blood pressure monitors that require validation of performance and labeling requirements.

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
116729960

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Flexmed RBD003
FDA UDI
Class IIActive
Flexmed RBD001
FDA UDI
Class IIActive
Flexmed RBD002
FDA UDI
Class IIActive

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