The ApneaLink Plus with easySense technology, a unique respiratory effort sensor, is a simple, low-cost portable home sleep test diagnostic device that records up to four channels of information. Screening for OSA (ApneaLink) - Resmed Middle-East. Me.resmed.com The ApneaLink software allows analysis of the AHI, oximetry, snore and flow limitation. Data is automatically analysed and the user is provided with a report. Plus, ApneaLink Air is compatible with our AirView TM, a comprehensive diagnostic software solution for sleep facilities.

General Information Technologies must be operated and maintained in accordance with Federal and Department security and privacy policies and guidelines. More information on the proper use of the TRM can be found on the.

Website: Description: ResMed ApneaLink hardware devices are sleep testing diagnostic products that offers patients the option of having a sleep test at home. The devices record respiratory effort, pulse, oxygen saturation and nasal flow, and reports apneas, hypopneas, flow limitation, snoring, blood oxygen saturation and the probability of Cheyne-Stokes respiration (CSR) breathing patterns.

The ApneaLink Air Software provides clinicians access to a more in-depth view of patients` recordings. This technology uses a proprietary database that saves files on the local computer. Note: There is not a dedicated website for this product but the product download can be found at the bottom of each ApneaLink hardware device page. Technology/Standard Usage Requirements: Users must ensure their use of this technology/standard is consistent with VA policies and standards, including, but not limited to, VA Handbooks 6102 and 6500; VA Directives 6004, 6513, and 6517; and National Institute of Standards and Technology (NIST) standards, including Federal Information Processing Standards (FIPS).

Users must ensure sensitive data is properly protected in compliance with all VA regulations. Prior to use of this technology, users should check with their supervisor, Information Security Officer (ISO), Facility Chief Information Officer (CIO), or local Office of Information and Technology (OI&T) representative to ensure that all actions are consistent with current VA policies and procedures prior to implementation. Section 508 Information: Section 508 does not apply. This product is considered Medical Technology as defined by the VA in the Medical Device Isolation Architecture (MDIA).

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For additional information or assistance regarding Section 508, please contact the Section 508 Office at Section508@va.gov. Decision: Decision Constraints: Veterans Affairs (VA) users must ensure VA sensitive data is properly protected in compliance with all VA regulations.