- September 24, 2015: Class II or I implants and life-supporting/ sustaining devices (Astral™, Stellar™, ResScan™).
- September 24, 2016: Rest of Class II devices (majority of ResMed products). Class II device labels and packages must bear a unique device identifier, and the data be entered into the GUDID.
- September 24, 2018: Class I devices – ResMed has very few Class I devices, but they too will contain UDI labeling.
Please contact our Customer Service department for more information.