Built around measurable decisions
Getinge focuses this site on dental equipment, patient monitoring, and infection-control products that hospitals, ASCs, and clinics can evaluate with clear evidence gates—not slogans.
Evaluation horizon
These gates describe how a facility can evaluate innovation. They are not release dates or regulatory claims for a specific Getinge product.
Software bill of materials requested for connected monitors and digitally controlled sterilizers where software is in scope.
Bidirectional identity and observation checks with Epic, Cerner, and MEDITECH environments where contracted.
Buyer teams document predetermined change control expectations for AI-enabled or software-updating modules.
Field visits focus on hardware unboxing while configuration and verification can be remote where validated.
Energy and CO2 planning become standard inputs in sterilizer and washer fleet replacement models.
Context, not nostalgia
Risk-based quality-system expectations became central to supplier review.
EU clinical evaluation and lifecycle obligations reshaped infection-control documentation.
Unique device identification became a go-live and recall communication requirement.
FDA expectations made secure product development and update planning procurement issues.
Teams evaluate devices, data pathways, service, and consumables as one operating system.
Interoperability ecosystem
These are standards and stakeholder systems, not partnership endorsements.
Co-development starts with constraints
Describe the current workflow, failure mode, intended users, data or reprocessing destination, and evidence required for a decision.
Open the Capability framework