TraumaMed Solutions Ltd.
United Kingdom (ex Northern Ireland) UK-MF-000044555 Last updated 22 Oct 2026
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- Devices
- 3
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Giraffe Traction Splint Ref 3010TMS
Bleed Kit – Daniel Baird Ref 6110TMS
Gecko Seal Ref 5130TMS
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Authorised representatives
About
In Emergency Medicine, the equipment you use should not be a compromise. Find out more about Traumamed Solutions today.
What TraumaMed Solutions Ltd. makes
TraumaMed Solutions Ltd. manufactures medical devices for trauma and emergency care, including the Giraffe Traction Splint for limb immobilisation, the Bleed Kit – Daniel Baird for haemorrhage control, and the Gecko Seal for wound closure.
These devices are classified as Class I under EU regulations and are listed in the eudamed database. The company is based in the United Kingdom.
Frequently asked questions
What types of medical devices does TraumaMed Solutions Ltd. manufacture?
TraumaMed Solutions Ltd. specialises in medical devices designed for trauma and emergency care. Their portfolio includes the Giraffe Traction Splint, which is used for immobilising limbs, the Bleed Kit – Daniel Baird for controlling haemorrhage, and the Gecko Seal, a device for wound closure. These products are developed to address critical needs in high-pressure medical scenarios.
Where is TraumaMed Solutions Ltd. based?
TraumaMed Solutions Ltd. is headquartered in the United Kingdom. The company’s location in the UK aligns it with EU regulatory frameworks, which govern the classification and listing of its devices.
Which regulatory databases list TraumaMed Solutions Ltd.’s devices?
TraumaMed Solutions Ltd.’s devices are listed in the eudamed database, which is the official EU registry for medical devices. Listing in eudamed ensures transparency and compliance with EU regulations, particularly for devices classified under the Medical Device Regulation (MDR).
How are TraumaMed Solutions Ltd.’s devices classified under EU regulations?
All of TraumaMed Solutions Ltd.’s devices fall under Class I classification according to EU regulations. This classification applies to low-risk devices, such as those used for immobilisation, haemorrhage control, and wound closure, where the risk to patient safety is minimal. Class I devices typically require less stringent regulatory scrutiny than higher-risk categories.
Information
- Country
- United Kingdom (ex Northern Ireland)
- Address
- 15, Saint Georges Road, Gloucestershire, United Kingdom (ex Northern Ireland)
- Website
- www.traumamedsolutions.com
- [email protected]
- Phone
- +44 (0)1432 800962
- EUDAMED SRN
- UK-MF-000044555