ITU-T H.850.6 PDF

The scope of this Recommendation¹ is to provide a test suite structure (TSS) and the test purposes (TP) for the Personal Health Devices interface based on the requirements defined in the Continua Design Guidelines (CDG) [ITU-T H.810 (2016)]. The objective of this test specification is to provide a high probability of interoperability at this interface.

The TSS and TP for the Personal Health Devices interface have been divided into the parts specified below. This Recommendation covers Part 10F.

– Part 1: Optimized exchange protocol. Personal Health Device

– Part 2: Optimized exchange protocol. Personal Health Gateway

– Part 3: Continua design guidelines. Personal Health Device

– Part 4: Continua design guidelines. Personal Health Gateway

– Part 5: Device specializations. Personal Health Devices interface. This document is divided into the following subparts:

• Part 5A: Weighing scales

• Part 5B: Glucose meter

• Part 5C: Pulse oximeter

• Part 5D: Blood pressure monitor

• Part 5E: Thermometer

• Part 5F: Cardiovascular fitness and activity monitor

• Part 5G: Strength fitness equipment

• Part 5H: Independent living activity hub

• Part 5I: Adherence monitor

• Part 5J: Insulin pump

• Part 5K: Peak expiratory flow monitor

• Part 5L: Body composition analyser

• Part 5M: Basic electrocardiograph

• Part 5N: International normalized ratio monitor

• Part 5O: Sleep apnoea breathing therapy equipment (SABTE)

• Part 5P: Continuous glucose monitor (CGM)

– Part 6: Device specializations. Personal Health Gateway 

– Part 7: Continua Design Guidelines. BLE Personal Health Device

– Part 8: Continua Design Guidelines. BLE Personal Health Gateway

– Part 9: Personal Health Devices Transcoding Whitepaper. Personal Health Devices

– Part 10: Personal Health Devices Transcoding Whitepaper. Personal Health Gateway. In addition to the main part, the document is subdivided into the following subparts:

• Part 10A: Whitepaper Thermometer requirements

• Part 10B: Whitepaper Blood pressure requirements

• Part 10C: Whitepaper Heart rate requirements

• Part 10D: Whitepaper Glucose meter requirements

• Part 10E: Whitepaper Weighing scales requirements

• Part 10F: Whitepaper Pulse oximeter requirements

• Part 10G: Whitepaper Continuous glucose monitoring requirements

¹ This Recommendation includes an electronic attachment with the protocol implementation conformance statements (PICS) and the protocol implementation extra information for testing (PIXIT) required for the implementation of Annex A.