Adequate labeling for a medical device requires proper design and procurement of the labels and labeling.
Medical device label printers.
Design includes labeling content that meets the requirement of the qs regulation as well.
Total visibility into the medical device labeling process.
Bartender labeling software lets you know who accessed a label what edits were made where and when a label was printed.
Many medical device manufactures chose to print labels in house to avoid label shortages caused by printing mistakes or regulation changes.
Additionally with healthcare organizations working toward implementing the newest technologies it is important for any and all medical device labels to be accurate and current.
Food and drug administration s fda new udi labeling requirements challenge manufacturers to redesign their labeling process and medical device udi labels.
Our label printing services take into account the many and varied environments medical device labels may be subjected to during packaging shipping storage and eventual use.
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.
Moisture resistant labels labels able to withstand extreme temperatures and more are available.
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.
Medical device udi unique device identifier labels easy medical device udi label compliance with the quicklabel ql 120x printer and robar software.
By digitizing your label production process you can meet regulatory requirements faster reduce labor costs get products to market faster and avoid recalls.
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.
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.
Capture e signatures and complete audit trail for compliance with global regulations including fda 21 cfr part 11.