AI-powered clarity in a fragmented safety landscape.
Centralized intelligence for early detection and prioritization of medical device risks.
Shaped with input from clinicians, biomedical engineers, and medical suppliers.
The challenge: safety data flows through fragmented pathways
Fragmented signals
Safety information is distributed across multiple systems and channels, making it challenging to maintain one coherent view of device-related developments.
Hard to classify and prioritize
Different types of safety updates vary in detail, timing, and relevance, which makes structured assessment and prioritization more complex within fast-paced operational environments.
Operational uncertainty
When information is dispersed, it becomes more difficult to anticipate customer needs, plan field activities, and allocate resources with full confidence.
Why unified safety intelligence matters
Global Context
injuries each year are associated with device-related adverse events worldwide, underscoring the operational and clinical importance of timely safety awareness.
annual deaths are linked to device-associated incidents, reinforcing the need for stronger post-market insight across the ecosystem.
in global healthcare costs are attributed to device safety events, affecting manufacturers, suppliers, and service networks across markets.
Regional Context
of ICU nurses in a national study reported encountering device-related challenges during clinical use, highlighting the pressure placed on service and supply partners.
reported having no clear visibility into a national pathway for escalating or reporting adverse events, creating gaps in coordinated response.
Many facilities still depend on manual logs and delayed safety updates, creating uncertainty and limiting the speed at which suppliers can support customers.
Global Context
Regional Context
injuries each year are associated with device-related adverse events worldwide, underscoring the operational and clinical importance of timely safety awareness.
of ICU nurses in a national study reported encountering device-related challenges during clinical use, highlighting the pressure placed on service and supply partners.
annual deaths are linked to device-associated incidents, reinforcing the need for stronger post-market insight across the ecosystem.
reported having no clear visibility into a national pathway for escalating or reporting adverse events, creating gaps in coordinated response.
in global healthcare costs are attributed to device safety events, affecting manufacturers, suppliers, and service networks across markets.
Many facilities still depend on manual logs and delayed safety updates, creating uncertainty and limiting the speed at which suppliers can support customers.
AEMS unifies device safety information through AI-driven classification and recall intelligence, giving organizations a single, structured view to support faster, more confident decisions.
What AEMS gives your organization
AI-driven classification
AEMS uses AI to categorize safety signals by severity and relevance (Critical / Moderate / Low).
Consolidated recall awareness
Relevant recall notices and safety updates appear in one structured interface instead of scattered channels.
Risk prioritization
Critical and high-impact issues surface clearly so teams can focus their effort where it matters most.
Device & site impact visibility
Clarifies which devices and locations may be affected, supporting faster, more targeted responses.
Coordinated follow-up workflow
Ownership, notes, and progress for each issue are tracked in one place, reducing miscommunication.
Structured documentation trail
A clear record of alerts, decisions, and actions supports audits, internal reviews, and compliance.
Built for hospitals, clinical teams, and industry partners
Hospitals & Clinical Departments
- •Clinical engineering & biomedical teams
- •Risk, quality, and patient safety units
- •Operations and safety review committees
AEMS gives hospital teams clearer visibility into device-related safety signals, AI-supported classification, and recall information to support prioritization, follow-up, and documentation.
Suppliers & Manufacturers
- •Medical device suppliers & distributors
- •Regional agents & service partners
- •Manufacturers monitoring field performance
AEMS helps suppliers identify relevant recalls and safety signals, coordinate communication with customer sites, and demonstrate structured, data-informed safety practices.
How AEMS fits into your safety workflow.
Connect your device portfolio
AEMS organizes your devices into a structured, searchable view aligned with your environment.
AI organizes relevant safety signals
Safety alerts, recall notices, and incident patterns are classified by severity and relevance to your devices.
Teams act with clarity and alignment
Priority issues, follow-up steps, and documentation are centralized, keeping stakeholders coordinated.
Industry insight from the field
“We want clarity on which device issues truly require action, not more noise and notifications.”
— Clinician
“It's critical to have a structured way to manage recalls and track follow-ups across sites.”
— Biomedical Engineer
“Downtime is expensive. We need better visibility to plan and prioritize maintenance decisions.”
— Operations Director
“We want to know exactly which customers are affected by a recall so we can reach out confidently.”
— Supplier
AEMS is built as an intelligence layer for modern healthcare operations, strengthening device safety oversight, elevating compliance readiness, and enabling confident, data-supported decisions across hospitals and suppliers.
Request access to AEMS
We partner with hospitals, clinics, and suppliers that want a unified, AI-supported view of device safety, classification, and recalls. Fill out the form below to submit your access request.