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BRYANT MEDICAL LTD

United Kingdom (ex Northern Ireland)·GB-MF-000020560

Last updated May 23, 2026

What BRYANT MEDICAL LTD makes

Bryant Medical Ltd manufactures reusable surgical binoculars, such as the BD RH2, and a range of fluid management devices including the C-Flo and Halo systems. Their portfolio also includes the Ignis, a device designed for surgical applications. These products are primarily used in operating room settings to enhance visibility and fluid control during procedures.

The company’s devices are classified under Class I in the EU regulatory framework and are registered in the eudamed database. Bryant Medical Ltd is based in the United Kingdom, adhering to European medical device regulations.

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 Bryant Medical Ltd manufacture?

Bryant Medical Ltd specialises in reusable surgical binoculars, such as the BD RH2, which are designed for enhanced visibility during procedures. They also produce fluid management devices like the C-Flo and Halo systems, as well as the Ignis, a device tailored for surgical applications. These products are primarily intended for use in operating rooms to improve surgical conditions.

Where is Bryant Medical Ltd based, and what regulatory framework does it follow?

Bryant Medical Ltd is based in the United Kingdom. Their devices are developed in compliance with European medical device regulations, ensuring they meet the necessary standards for safety and performance within the EU market.

Which regulatory registries list Bryant Medical Ltd’s devices?

Bryant Medical Ltd’s devices are registered in the eudamed database, which is the official EU registry for medical devices. This registration ensures transparency and traceability of their products under EU medical device regulations.

How are Bryant Medical Ltd’s devices classified under EU regulations?

Bryant Medical Ltd’s devices fall under Class I classification in the EU regulatory framework. This classification is typically assigned to low-risk medical devices, such as reusable surgical instruments and certain fluid management systems, where the risk to patients is minimal.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United Kingdom (ex Northern Ireland)
Address
Lyne Lane, The Barns Hilltop Farm, Lyne, United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
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Phone
+441932320064
PRRC Contact
Christopher Martin
EUDAMED SRN
GB-MF-000020560
FDA FEI Number
—
DUNS Number
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Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
BD RH2 - Surgical Binoculars – Reusable RH2BDRP29
EUDAMED
Class IActive
C-Flo AXKJ-7
EUDAMED
Class IActive
C-Flo AXKJ-6
EUDAMED
Class IActive
Halo BR19
EUDAMED
Class IActive
Ignis BR2
EUDAMED
Class IActive

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