1 June The Coding & Marking Technologies of the Medical Devices Sector With the latest roll out of the EU Medical Devices legislation, it is important to uncover the latest in coding and marking technologies. Depending on the medical device and the coding surfaces involv...
22 May The Role of Coding & Marking in the Medical Devices Sector Based on manufacturer prices, the European medical technology market is worth €110 billion and is estimated to make up 28% of the world market, making it the second largest in this sector after the US...
22 May UFI regulation and the coding technologies that will help Under new EU legislation, manufacturers of products that contain hazardous mixtures must add a special sixteen-digit code to their product labelling. Here’s an introduction to the upcoming regulations...
8 May EU Medical Devices Legislation: What is it & how does it affect me? The term ‘medical device' covers a broad range of items. Mainly it is referred to as an apparatus or a piece of equipment that is used to treat or diagnose a condition which comes into direct contact ...
30 April 5 further ways the N610i label press can enhance your profits The N610i isn’t just a market leading label press in terms of quality. It delivers compelling business benefits that could enhance your profits. ...
18 April New legislations & staying compliant in the medical devices sector – an audience with Volker Watzke In the past, there was very little need for medical device identification. With the adoption of the upcoming EU Medical Device Regulation (MDR) this will all change. We spoke with Volker Watzke, Domin...
10 April How has UDI affected the US medical devices market? Paul Hammond gives his insights. The US medical devices market has experienced a major change since the introduction of the Food and Drug Administration (FDA) UDI ruling back in September 2014. We spoke with Paul Hammond, Domino’s Me...
28 March Label serialisation – choosing the correct coding technology for the US DSCSA compliance Medicines for the US market are predominantly packed in bottles, with statutory information printed on labels affixed to these bottles. As Pharmaceutical manufacturers are gearing up to meet the DSCSA...