Medical Quality Product

DRI Sleeper® alarms are designed and manufactured in New Zealand by Anzacare Limited and are registered as, and compliant with, medical device regulations in USA, UK, Europe, Australia and New Zealand.

The device listing number with FDA is A808527.

The device listing number with ARTG is 276585.

DRI Sleeper alarms carry the CE (European Conformity) mark which indicates conformity with health, safety and environmental protection standards for products sold within the European Economic Area.