U.S. FDA Medical Device Establishment Registration

August 8, 2023

We are delighted to announce that our registration with the US Food & Drugs Agency (FDA) is now active. Every establishment that manufactures, repacks, or re-labels drug products in the United States is required to register with the FDA.

We look forward to supplying our range of EURIECA® Response Bags and other items of advanced  first aid equipment to clients in the US.

All of the equipment that we supply is sourced from world-leading manufacturers, with every item on the Trauma Resus approved equipment list having a clear objective based upon clinical effectiveness, ease of use in challenging environments, high levels of skill retention, and value for money.

Please click here to validate the Trauma Resus FDA Registration.