Enterprise application areas D46

Infrared vision development services for medical, nursing and human thermal physiology research

For equipment manufacturers, system integrators and enterprise R&D related to "medical treatment, nursing and human thermophysiology research", it provides infrared data evaluation, algorithm development, equipment/platform integration and test acceptance, covering 8 types of enterprise application scenarios.

Service scope and implementation plan

direction numberD46
Demand scenario8 items
main inputMedical radiation type LWIR L2;
Typical routeT16、T20

The project scope is determined based on samples, equipment, working conditions and written indicators; general modules, special models and multi-sensor integration are configured according to the evaluation results.

Application scenarios and development content

IR361

Controlled environment frontal/medial canthus skin temperature screening

Minimum input and technical route
Medical radiation type LWIR L2;T16
target output
Individual surface temperatures and retest tips
Implementation
Medical device path required
critical acceptance
According to IEC 80601-2-59/local regulations and clinical evaluation; does not diagnose infection
IR362

Auxiliary study on left-right temperature difference and ulcer risk in diabetic foot

Minimum input and technical route
LWIR L2/L3;T16
target output
Plantar zone temperature, symmetry and trends
Implementation
Need clinical research
critical acceptance
Sensitivity/specificity compared to standard clinical assessment
IR363

Assisted observation of early thermal abnormalities in pressure injuries

Minimum input and technical route
LWIR L2/L3;T16
target output
Skin ROI Temperature difference and longitudinal changes
Implementation
Need clinical research
critical acceptance
Comparison with nursing stage/follow-up outcomes
IR364

Study on burn, wound and postoperative perfusion thermal patterns

Minimum input and technical route
LWIR L2/L3;T16
target output
Symmetry, hot and cold spots, and recovery curves
Implementation
Need clinical research
critical acceptance
Compared with perfusion/clinical outcomes; adjuvant only
IR365

Thermal symmetry study of inflammation, joint and muscle damage

Minimum input and technical route
LWIR L2/L3;T16
target output
ROI temperature, left and right difference and recovery trend
Implementation
Need clinical research
critical acceptance
Subject preparation, environmental control, reproducibility
IR366

Non-contact study of respiratory airflow and respiratory rate

Minimum input and technical route
Close range LWIR/MWIR L3;T16
target output
Nose and mouth heat flow waveform and frequency
Implementation
Requires controlled research
critical acceptance
Comparison with breathing belt/pulmonary function equipment
IR367

Study on peripheral perfusion and cold stimulation rewarming curves

Minimum input and technical route
LWIR L2/L3;T16
target output
Rewarming time, slope and symmetry
Implementation
Ethics/clinical design required
critical acceptance
Compared to blood flow/standard examination, repeatability
IR368

Standardized collection, desensitization and review of medical thermal images

Minimum input and technical route
L2/L3;T20
target output
Subject preparation, environment, ROI, version and audit
Implementation
Quality system required
critical acceptance
Protocol compliance rate, cross-operator consistency

Information required before project evaluation

  • Target equipment/object, site conditions, business processes and follow-up actions to be taken
  • Infrared camera, lens, spectral band, installation distance, field of view, resolution and data interface
  • Original samples and collection parameters under normal, abnormal, boundary and interference conditions
  • Reference truth values and annotation specifications for temperatures, parts, states, or events
  • Target platform, network, interface, storage, latency and operating resource constraints
  • False positives, missed negatives, manual review, linkage, failure handling and acceptance thresholds

Implementation and delivery methods

  1. Project input confirmationCheck camera, spectral band, bit depth, SDK, environmental conditions, sample and acceptance true value.
  2. Sample verificationVerify key processing links, applicable conditions and abnormal working conditions, and determine the development scope and acceptance methods.
  3. Algorithm development and integrationImplement data parsing, algorithms, quality gating, interfaces and target platform deployment.
  4. Test acceptance and handoverRetest according to the agreed test set and target platform, and hand over the deliverables, test results and applicable conditions.
  • Requirements and technical solutions, input and output and interface field definitions
  • Algorithm library, model or SDK/API; delivery form is confirmed in the project plan
  • Sample program, parameter configuration, error status and calling instructions
  • Test set version, indicator definition, stratification results and failed sample records
  • Target platform adaptation, resource usage and running delay records
  • Version, dependencies, license, reproduction steps and applicable conditions description

Acceptance design

Each scenario establishes independent test cases according to "key acceptance". When sharing models across scenarios, results are reported separately for each scenario, distance, load, environment, and target size, supplemented by overall statistics.

When high-risk alarms or controls are involved, the algorithm output is used for review or linkage judgment; safety functions, regulatory responsibilities, and automatic disposal require separate design and acceptance.

Frequently Asked Questions for Enterprise Customers

Can I purchase directly based on one of the scenes?

Can be evaluated first as a separate work package. The formal scope should describe the device, data, target objects, environment, interfaces, delivery form, and acceptance thresholds.

Can it be started when there are no abnormal samples?

The data interface, normal baseline, acquisition plan and simulation/controlled test design can be completed first; the abnormal detection rate and fault classification effect can be evaluated after obtaining sufficient abnormal true values.

Can the algorithm directly trigger alarms or equipment actions?

Duration, deduplication, quality gating, manual review, communication failure and safety interlocking need to be designed based on business risks. High-risk actions should be activated after completion of independent safety mechanisms and on-site acceptance.

Project consultation

Define the Development Scope with Samples and Device Requirements

Infrared vision development services for medical, nursing and human thermal physiology research

Please describe the task object, original picture or video, target indicators, device platform, interface and sample situation.

Phone: 13910119357
xuzhiyang0928@gmail.com

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