The BioRadio is intended for use in education and research applications only. The BioRadio is not FDA cleared to market. It is not intended for use in experimentation that involves human testing without specific IRB approval. The BioRadio is CE marked and has been developed and is manufactured under quality system regulations that follow ISO13485 Quality System Requirements. Great Lakes NeuroTechnologies has ISO certification as part of our quality system in manufacturing. View Certification.

The BioRadio complies with the Radio and Telecommunications Terminal Equipment (R&TTE) Directive 1999/5/EC and the Electromagnetic Compatibility (EMC) Directive 2004/108/EC which are part of the product electrical safety requirements stated within IEC 60601-1. Compliance to these two requirements and having a certified QMS (Quality Management System) allow us to declare conformity to the applicable directives and place the CE mark on the BioRadio and associated software and accessories for the above intended use.

 

The BioRadio is intended for use in education and research applications only. The BioRadio has not yet been reviewed, certified, or approved by the FDA or similar organization for use with patients or clinical purposes. In no case should the BioRadio be used for any diagnosis, treatment or other medical decision-making purposes. All use of the BioRadio must be in compliance with 45 CFR 46 and appropriate human subjects’ procedures as they exist within your institution.