The UDI is a set of numeric or alphanumeric characters produced by a device identifying and coding standards recognized internationally. It enables the clear identification on the market of certain medical equipment. A Unique Device Identification (UDI) system intends to deliver the distribution and operation of a single, globally harmonized identification of medical devices, which requires a standard UDI-D label of devices (for conveying automatic identification and data capture and, if applicable, their Human Readable Interpretation)
There are lots of benefits to implementing the UDI system. It aims to improve patient safety, modernize the monitoring of devices, and facilitate innovation in medical devices. UDI helps to track goods and their manufacturer. The ID must be read in human as well as machine forms.
Listed below are some of the benefits of integrating the UDI system
- They help in the fast discovery of faulty medical devices
The food and drug administration receives reports of faulty medical devices. Therefore, they receive a huge amount of reports yearly and have to determine the valid ones, single flawed and which contain a pattern of defects. Therefore, medical services are often uncertain about whose provider they get the defective medical equipment and the fabrication date or batch number. The medical system provides these reports. This severely impedes the FDA’s ability to assess whether a reported medical device defect is a single event or a pattern. UDI will ensure that if malfunctioning medical equipment is detected, the UDI label indicates exactly where the item comes from and, in some cases, its batch number and expiration date. Therefore, the FDA can cross reference number UDIs and spot trends quickly when it gets medical device reports through the UDI system. This decreases the timeline between the initially failed device identification, and the Unique Device Identification System significantly reduces retrieval determination.
- It reduces medical errors
The Unique Device Identification allows healthcare practitioners to identify medical equipment by supplying detailed device features correctly. This reduces time and eliminates misunderstanding with different versions of medical devices. Additionally, clear labeling provides an extra verification level before the application or implantation of a medical device in a patient. This additional verification helps avoid blending, which might cause fatalities. In some circumstances, UDI can also ensure that the expiry date is clearly shown in specific medical devices instead of being recorded on the box that the medical device was supplied in.
- Provides a better assessment of device performance
UDI produces a huge number of trackable data for medical devices. Medical device information may be utilized to build real-time cost, recall and waste analysis by establishing common terminology. Physicians can evaluate medical implants using the device type. The implant has been implemented at this facility, and sometimes the doctors have carried out the intervention to assess the health results.
- Faster recalls
In case of medical faults, then action needs to be taken as fast as possible. However, the FDA may take a long to determine the date and origin of defective devices and notify the patient of a recall, the greater the danger of injury or death. The process will be slow if you do not have \udi. However, with the use of UDI, Medical professionals may quickly verify whether medical devices are included in a callback and remove these devices from usage. UDI removes any conjecture so that hospitals no longer have to conjecture which medical equipment the afflicted manufacturer had come from during the reclamation date. You scan a barcode and know for sure if the gadget is retrieved.