iArmoni digitalises the complete circuit of surgical material, inside and beyond the hospital — planning, use, reprocessing and stock — and turns it into intelligence for the hospital and its ecosystem.
Trusted by leading European hospital groups, public reference hospitals and a global medtech manufacturer.
One connected circuit across every hospital, manufacturer and supplier. One data layer for the entire ecosystem.
THE CHALLENGE
Every station — sterile processing, theatre, stock — and every provider — material, supplies, external sterilisation — runs on its own tools, paper records and partial traceability. No one owns the complete circuit, so no one can turn it into decisions.
Paper-based verification leaves room for human error. Verification gaps expose patients to infection risk.
A partial, decentralised record cannot meet a quality audit or answer a health alert.
Material processed and never used. Instruments lost. Urgent shipments for want of foresight.
THE PLATFORM
Every item, every cycle, every action, every person responsible — recorded, time-stamped, auditable.
THE OUTCOME
The material used on each patient, with its full handling history and sterility assurance.
Audit-ready records in real time, automatic reports. Aligned with MDR 2017/745.
Every instrument identified, located and individually audited, in real time.
By surgical procedure, material reference and hours of use. Requested vs actually used.
THE NETWORK
One hospital: the complete record of its surgical material.
Around each hospital: its HIS, its equipment park from any manufacturer, its external sterilisation operator, its material suppliers. Data that crosses actors — what none of them sees alone.
Across hospitals, surgical procedures and material types, anonymised: benchmarks, real cost per procedure, demand patterns. Data that compounds.
REFERENCES
18 theatres, central sterilisation and 100+ daily professional users. Awarded by public tender, integrated with SAP.
Multi-site roll-out across its centres.
Shared consignment stock across its hospitals, on iArmoni.
The MDR mandates a permanent, machine-readable UDI on every reusable device (MDR 2017/745, Art. 27 and 123(3)(g); reusable Class I from 26 May 2027). Marking is only the start: to be traceable and compliant, every read has to be registered. iArmoni automates that record — and turns the data into traceability, safety and cost control.
