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Sign in to claim this brandBRYANT 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)
- Website
- www.bryant.dental
- —
- —
- [email protected]
- Phone
- +441932320064
- PRRC Contact
- Christopher Martin
- EUDAMED SRN
- GB-MF-000020560
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (5)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| BD RH2 - Surgical Binoculars – Reusable | RH2BDRP29 | EUDAMED | Class I | Active |
| C-Flo | AXKJ-7 | EUDAMED | Class I | Active |
| C-Flo | AXKJ-6 | EUDAMED | Class I | Active |
| Halo | BR19 | EUDAMED | Class I | Active |
| Ignis | BR2 | EUDAMED | Class I | Active |
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