TouchMark Blog

TouchMark’s expertise includes medical device pad printing in multiple categories of FDA classification.

Tom Waits once sang of a character named Small Change, who apparently “got rained on with his own .38,” and device makers might sometimes have felt as though small changes to their devices didn’t always work out so well, either.

Many of FDA’s Unique Device Identification requirements have already phased in. The labels and packages of Class III and Class II medical devices

Textures vary according to their individual depth, the degree of draft on the sidewalls, and the frequency of peaks and valleys for a given surface area. Some textures are more difficult to print successfully than others, and there are certain textures that are simply impossible to cover completely.

Although polymers have suffered through some tough media disparagement as of late (biodegradability issues) it is highly unlikely that these polymers are replaceable for medical device manufacturing. These specialized materials are indispensible for providing low cost but effective vehicles for delivering everything from successful operating techniques to therapeutic medicines.

Medical tubing has evolved to be a complex, sophisticated product combining various materials, technologies and processes

Medical tubing has evolved to be a complex, sophisticated product combining various materials, technologies and processes.  

Medical grade inks used to mark medical devices should meet important safety standards. The United States Pharmacopoeia (USP) 30, NF 25, 2007 standard also known as Class VI is widely used to comply with stringent FDA rules for products that come in contact with the human body.