Complete traceability of medical instruments, implants, devices and consumables means greater safety for the patient.
A relevant step in UDI implementation in Europe is mandatory UDI-carrier placement on implantable and class III devices starting May 2021 in accordance with Regulation (EU) 2017/745 (MDR - Medical Device Regulation). Reliable identification and data acquisition systems are an important basis to allow manufacturers, distributors and users to meet the new requirements.
This white paper gives you an overview of the UDI regulations and the various technical solutions for marking and automatic identification of medical devices.
Learn how to comply easily with UDI marking requirements on medical devices bringing benefits to all involved - including:
and many others.
Download your complimentary White Paper by filling out the form
Datalogic Scheduled Maintenance, May 19th, 1.00 AM/2.00 AM (CET)
Datalogic wants to make you aware that on May 19th, 1.00 AM/2.00 AM (CET), there will be scheduled down time for approximately one hour.
We will be using this time to add more capacity to our infrastructure and speed up our overall service.
During this maintenance window, our Corporate Website (datalogic.com), Partner Portal (Extranet) and all the related services will be inaccessible.
All system functionalities will resume immediately after the maintenance window.
We appreciate your patience and understanding.