Medical device udi unique device identifier labels easy medical device udi label compliance with the quicklabel ql 120x printer and robar software.
Medical device label printers.
Bartender labeling software lets you know who accessed a label what edits were made where and when a label was printed.
With over 80 barcode types and pre configured label samples teklynx udi labeling software is capable of printing the health industry bar code hibc and gs1 barcodes required for udi compliance with support for thermal and thermal transfer printers.
Lms enterprise enables medical device manufacturers to use a single software platform for all printing devices and for all packaging and shipping from primary to tertiary labeling.
It also excludes the need to hold labels in stock.
Design includes labeling content that meets the requirement of the qs regulation as well.
Adequate labeling for a medical device requires proper design and procurement of the labels and labeling.
Total visibility into the medical device labeling process.
By digitizing your label production process you can meet regulatory requirements faster reduce labor costs get products to market faster and avoid recalls.
Food and drug administration s fda new udi labeling requirements challenge manufacturers to redesign their labeling process and medical device udi labels.
Our in house printing solutions increase production flexibility by allowing quick label changes to be updated on demand using the neuralabel 300x printer and the neuralabel 500e printer.
Using a third party company for printing could cause your business to wait weeks at a time for new medical device labels to be created and sent back to you.
The ql 120x label printer dramatically reduces the costs of udi compliant and medical device labels eliminates the risk of using obsolete labels or choosing the wrong label from inventory.
Moisture resistant labels labels able to withstand extreme temperatures and more are available.
Many medical device manufactures chose to print labels in house to avoid label shortages caused by printing mistakes or regulation changes.
Capture e signatures and complete audit trail for compliance with global regulations including fda 21 cfr part 11.