TouchMark Blog

April 10, 2019

Meeting FDA Compliance Standards in printing Class I, Class II and Class III Devices

TouchMark’s expertise includes medical device pad printing in multiple categories of FDA classification.
October 27, 2017

Small Changes; FDA and the 510(k)

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.
June 12, 2017

5 ongoing challenges for UDI

Many of FDA’s Unique Device Identification requirements have already phased in. The labels and packages of Class III and Class II medical devices
May 11, 2017

Pad Printing On Textured Surfaces

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.
April 11, 2017

The RX Factor – Medical Plastics And Adhesion

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.
March 11, 2017

Tubing’s Constant Evolution

Medical tubing has evolved to be a complex, sophisticated product combining various materials, technologies and processes
November 30, 2016

Tubings Constant Evolution

Medical tubing has evolved to be a complex, sophisticated product combining various materials, technologies and processes.  
September 22, 2016

The Importance of Medical Grade Ink

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.
April 10, 2019

Meeting FDA Compliance Standards in printing Class I, Class II and Class III Devices

TouchMark’s expertise includes medical device pad printing in multiple categories of FDA classification.
October 27, 2017

Small Changes; FDA and the 510(k)

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.
June 12, 2017

5 ongoing challenges for UDI

Many of FDA’s Unique Device Identification requirements have already phased in. The labels and packages of Class III and Class II medical devices
May 11, 2017

Pad Printing On Textured Surfaces

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.
April 11, 2017

The RX Factor – Medical Plastics And Adhesion

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.
March 11, 2017

Tubing’s Constant Evolution

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