Product Catalog

Localized Clinical AI Appliances & Peripherals

Explore deployment-ready product categories for controlled pilots and stakeholder evaluation. Commercial terms, proprietary architecture, and detailed integration materials are shared only through qualified enquiry.

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Medi AI Standard Edition

Clinical edge appliance

Medi AI Standard Edition

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Designed for outpatient clinics, consultation rooms, and general ward environments that need local clinical workflow support.

Medi AI+ Advanced Clinical Edition

Higher-acuity clinical appliance

Medi AI+ Advanced Clinical Edition

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Built for higher-acuity pilot environments where teams need expanded local compute, multimodal intake, and supervised bedside workflow documentation.

Radiology AI+ Advanced Imaging Edition

Radiology edge appliance

Radiology AI+ Advanced Imaging Edition

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Designed for imaging departments evaluating local AI-assisted radiology workflow support and controlled imaging review pilots.

Laboratory AI+ Advanced Laboratory Edition

Laboratory edge appliance

Laboratory AI+ Advanced Laboratory Edition

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Built for laboratory environments evaluating localized sample workflow organization and operational reporting support.

Telemed AI+ Remote Consultation Edition

Telemedicine edge appliance

Telemed AI+ Remote Consultation Edition

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Designed for remote consultation workflows where clinicians need secure video consultation, local patient context, and care-team coordination support.

Clinical Peripherals Kit

Peripheral bundle

Clinical Peripherals Kit

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A coordinated set of clinical input peripherals for pilot sites evaluating localized multimodal workflow documentation.

Pilot & Regulatory Notice

Product concepts and pilot configurations shown on this website are for stakeholder evaluation, controlled pilot planning, and qualified commercial discussion only. They are not represented as HSA-registered or approved medical devices, diagnostic systems, treatment systems, or substitutes for professional clinical judgement. Any Singapore deployment must undergo appropriate institutional review, clinical governance, cybersecurity assessment, procurement checks, PDPA/data protection review, and, where applicable, Health Sciences Authority (HSA) medical-device classification, registration, licensing, and approval processes before clinical or operational use.