Medical Devices & Healthcare IoT

RelayQ for FDA-regulated devices, patient monitoring, and medical IoT infrastructure.

The Problem

Medical device software must meet IEC 62304 (software lifecycle) and demonstrate risk management per ISO 14971. Every dependency in your MQTT broker is a risk item that requires analysis, monitoring, and mitigation documentation. Brokers with 200+ dependencies create an unmanageable risk register.

How RelayQ Solves This

Minimal risk surface. Zero runtime dependencies means your risk analysis for the communication component is one page, not fifty.

Deterministic behaviour. Thread-per-client model with no async runtime means no unpredictable scheduling delays. Critical for patient monitoring where message latency matters.

Auditable codebase. 1,100+ protocol tests with full coverage of the MQTT 3.1.1 specification. Your IEC 62304 auditor can verify coverage in a single session.

Key Features for Medical

FeatureBenefit
Zero dependenciesMinimal IEC 62304 risk items
Spec-traceable testsMaps to verification & validation requirements
Deterministic latencyPredictable message delivery for monitoring
mTLSDevice authentication for patient data
Default-deny ACLHIPAA-aligned access control
OOM protectionGraceful degradation, never crashes
< 50ms startupFast recovery after device power cycle

Deployment

  • Bedside gateway: 826KB binary on medical-grade ARM device
  • Hospital infrastructure: Docker container with TLS + ACL
  • Wearable hub: Embedded in OEM monitoring hardware

Next Steps

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