Hebei Sighture Medical Equipment Technology Co., Ltd.
Hebei Sighture Medical Equipment Technology Co., Ltd.
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Services

Remote Support
Remote Support
01
Global Technical Support

Our certified engineers provide 24/5 real-time diagnostics and troubleshooting via secure channels. Immediate intervention for hardware/software issues ensures minimal clinical disruption.

02
Proactive R&D Assistance

Developers deliver same-day software optimizations and OTA patches. Custom algorithm updates address site-specific operational challenges without on-site visits.

03
Continuous After-Sales Oversight

Dedicated teams monitor device performance remotely, scheduling predictive maintenance and security updates. Full audit trails guarantee compliance adherence.

Customized Diagnostic & Therapeutic Equipment Solutions
Customized Diagnostic & Therapeutic Equipment Solutions
R&D-Driven Custom Simplicity
R&D-Driven Custom Simplicity

Our engineers streamline customization with modular sensor platforms and OTA-updatable software. Clinical requirements transform into turnkey solutions within 8 weeks—zero coding expertise needed.

Market-Optimized Solutions
Market-Optimized Solutions

Marketing specialists refine your specifications into clinically viable products. We co-design compliance documentation, branding, and training protocols for seamless market entry.

Partnership Growth Focus
Partnership Growth Focus

Shared KPIs and IP flexibility ensure mutual success. Your market expansion fuels our innovation—proven by 30%+ client revenue growth in co-developed projects.

Sighture OEM/ODM Service

Tailored Medical Solutions

Sighture Medical delivers precision-engineered customization across all product lines:


Scenario-Specific Adaptation

Modify hardware specifications (sensor density, platform dimensions) and software protocols for unique clinical/research environments—rehabilitation, sports science, or academic studies.


Co-Development Partnership

Collaborate directly with our R&D team to develop proprietary algorithms, specialized interfaces, or integrated systems addressing unmet diagnostic or therapeutic needs.


End-to-End Custom Workflow


Phase 1: Requirements analysis + feasibility study

Phase 2: Prototype development & validation

Phase 3: Regulatory-compliant production

Phase 4: OTA-enabled lifetime support


ISO 13485 framework ensures quality rigor throughout customization processes.

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