Editorial Technical Reference

Patient Data Interface

This page explains how Patient Data Interface is classified within Computer, Electronic and Optical Product Manufacturing. Technical values and manufacturer relationships are research references; confirm the current specification and supplier evidence for each order.

Technical Definition & Core Assembly

Interface component for inputting and managing patient-specific data within the Dose Calculation Engine

Representative product image. Confirm appearance and specifications with the manufacturer.

Product Specifications

Technical details and manufacturing context for Patient Data Interface

Definition
The Patient Data Interface is a component of the Dose Calculation Engine that provides a secure and structured entry point for patient-specific information required for radiation dose calculations. It handles the input, validation, and management of clinical data such as patient demographics, anatomical details, treatment history, and diagnostic imaging references. The interface ensures that data is formatted and checked according to predefined clinical ranges and standards, maintaining integrity and compatibility with the engine's computational algorithms. It operates using standardized communication protocols, including HL7 FHIR R4, and supports Ethernet data transfer rates of 10–100 Mbit/s per IEEE 802.3. The interface is designed for indoor use with an IP20 rating, operates within a temperature range of 0–50 °C, and can be stored between -20 and 70 °C. It requires a non-condensing environment with relative humidity between 10% and 90%. Power consumption ranges from 5 to 15 W, and the operating voltage is 24 V DC ±10% per IEC 61131-2. The device dimensions are 100 x 30 x 120 mm (W x H x D), and it weighs between 0.5 and 1.0 kg. Data accuracy is ±0.1% relative to full scale, and response time for critical alerts is ≤10 ms. The interface is constructed with electronic components, a plastic housing, and copper wiring. It is important to verify model-specific values and standards with the legal manufacturer or supplier before procurement or use.
Working Principle
The interface receives structured patient data through standardized protocols, such as HL7 FHIR, and performs validation checks against predefined clinical ranges and formats. It employs error-checking algorithms and data normalization processes to ensure consistency and accuracy. After validation, the verified data is transmitted to the core calculation modules of the Dose Calculation Engine. The interface also manages data flow, ensuring that only complete and correct information is used for dose calculations. It operates within specified electrical and environmental limits, and its response time is optimized for critical alerts.
Common Materials
Electronic components, Plastic housing, Copper wiring
Technical Parameters
ParameterTypical rangeNotes & selection driver
Operating Voltage24 ±10% V DCStandard industrial supplyIEC 61131-2
Power Consumption5–15 WDepends on data throughput
Data Transfer Rate10–100 Mbit/sEthernet interfaceIEEE 802.3
Communication ProtocolHL7 FHIRHealthcare interoperabilityHL7 FHIR R4
Operating Temperature0–50 °CNon-condensing environmentIEC 60068-2-1, IEC 60068-2-2
Storage Temperature-20–70 °CProtect from extreme heatIEC 60068-2-1, IEC 60068-2-2
Relative Humidity10–90 %Non-condensingIEC 60068-2-78
Ingress Protection RatingIP20Indoor use onlyIEC 60529
Dimensions (W x H x D)100 x 30 x 120 mmCompact module
Weight0.5–1.0 kgLightweight for mounting
Data Accuracy±0.1 %Relative to full scale
Response Time≤10 msFor critical alerts

Ranges are indicative industry figures for RFQ preparation, not a supplier commitment. Confirm every value and standard with the legal manufacturer before ordering.

Components / BOM
  • Data Input Port Part
    Physical connection point for data transmission cables
    Material: Stainless steel
  • Processing Unit
    Validates and processes incoming patient data
    Material: Silicon semiconductor
  • Interface Board
    Circuit board that manages data flow between components
    Material: Fiberglass-reinforced epoxy

Applied To / Applications

This component is essential for the following industrial systems and equipment:

Industrial Ecosystem & Supply Chain Structure

Complementary Systems
Downstream Applications
Specialized Tooling

Application Fit & Sizing Matrix

Operational Limits
pressure: Atmospheric only (non-pressurized system)
other spec: Data throughput: 100-1000 patient records/hour, Network latency: <100ms, Uptime: 99.9%
temperature: 15°C to 35°C (operating), 0°C to 50°C (storage)
Media Compatibility
✓ HL7 v2.x healthcare data standards ✓ FHIR R4 API integrations ✓ DICOM medical imaging data
Unsuitable: High-EMI industrial environments without proper shielding
Sizing Data Required
  • Maximum concurrent user connections
  • Average patient data volume per record (MB)
  • Required integration frequency (real-time vs. batch)

Reliability & Engineering Risk Analysis

Failure Mode & Root Cause
Corrosion-induced leakage
Cause: Exposure to bodily fluids, cleaning agents, or environmental moisture leading to material degradation and seal failure at connection points.
Connector wear/fretting
Cause: Repeated insertion/removal cycles causing mechanical wear, contact oxidation, or pin misalignment, resulting in intermittent or lost data transmission.
Maintenance Indicators
  • Intermittent data transmission or frequent disconnection alerts during patient monitoring
  • Visible corrosion, discoloration, or residue buildup on connectors or cable entry points
Engineering Tips
  • Implement regular connector inspection and cleaning protocol using manufacturer-approved, non-conductive cleaning solutions to prevent corrosion and contact degradation
  • Establish controlled insertion/removal procedures with proper alignment and minimal force to reduce mechanical wear, and use protective caps when not in use

Indicative industry ranges for design and RFQ preparation. Confirm the exact figures and applicable standard with the manufacturer before specifying.

Compliance & Manufacturing Standards

Applicable Standards
IEC 62304:2006 - Medical device software - Software life cycle processes ISO 14971:2019 - Medical devices - Application of risk management to medical devices

Quoted from the published standard.

Manufacturing Precision
  • Data transmission accuracy: +/-0.1%
  • Interface response time: <100ms
Quality Inspection
  • Cybersecurity vulnerability assessment
  • Data integrity verification test

Manufacturers of Patient Data Interface

Manufacturer profiles associated with Patient Data Interface.

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Frequently Asked Questions

What is the operating voltage of the Patient Data Interface?

The operating voltage is 24 V DC with a tolerance of ±10%, according to IEC 61131-2. Always verify the exact requirement for your specific model with the manufacturer.

Which communication protocol does the interface support?

The interface supports HL7 FHIR R4 for healthcare interoperability. It also has an Ethernet interface with data transfer rates of 10–100 Mbit/s per IEEE 802.3.

What are the environmental operating conditions?

The interface is for indoor use only, with an IP20 rating. It operates in non-condensing conditions at temperatures from 0 to 50 °C and relative humidity from 10% to 90%. Storage temperature is -20 to 70 °C.

How accurate is the data processing?

Data accuracy is ±0.1% relative to full scale. Response time for critical alerts is ≤10 ms. These values are reference ranges and should be confirmed for your specific application.

Data Basis

Editorial classification, named public sources where available, and source-reviewed manufacturer records.

Preliminary Technical Classification
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