Automatic identification of products from reception to use.
UDI regulation requires knowing which product was used on each patient, and recording it by hand in the middle of clinical work is slow and error-prone.
The product is identified automatically, with no codes to type in the middle of clinical work.
Knowing which patients received an affected batch without searching through paper records.
The traceability required by regulation is recorded as part of everyday work.
When an alert arrives, affected material still in stock is located and the patients involved are identified, so the hospital can act quickly and keep a record.
To identify medical devices automatically, without scanning one by one, and record their receipt, location and use. It is particularly useful for implants and high-value devices.
Regulation (EU) 2017/745 on medical devices requires health institutions to record and keep the unique device identifier (UDI) of the class III implantable devices they supply or receive. We build that record into daily work.
Yes. Traceability data is integrated with the ERP and, where appropriate, with the patient episode, through interfaces agreed with the IT team.
Shall we talk about how it applies to your hospital?
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