Medical device manufacturers have historically built their products by focusing on function way before form. If usability and design are even considered, it’s an afterthought at best. Of course, some degree of complexity in medical devices is understandable. Sciessent, the leading provider of antimicrobial solutions, today announced its partnership with Compounding Solutions, a leader in the production of specialty compounds for the medical-device industry. Compounding Solutions will integrate Sciessent's A Colorado Springs company that manufactures medical devices for some of the biggest names in the business is in the midst of a growth spurt, thanks to burgeoning demand from its customers. By the end of 2015, CEA Medical Manufacturing will have increased The suit states, however, that the device-maker had responsibilities to patients such as Gomez. “The manufacturer must ensure that the validated reprocessing protocol is disseminated to medical facilities and professionals,” the suit states. Tijuana, Baja California – When Phase 2 Medical, Rochester, New Hampshire, a medical device contract manufacturer of single-use, started exploring the idea of expanding their operations to a cost effective location the company was set to go to Costa Rica. Evana Automation Specialists, a leading Systems Integrator and builder of custom, automated assembly and test systems, recently shipped a robotic material handling system to a prominent medical device manufacturer. The Evana solution will transport wire .
are outlined in a final industry guidance aimed at helping device manufacturers develop safer reusable devices, especially those devices that pose a greater risk of infection. Medical devices intended for repeated use are commonplace in health care Two major diabetes associations have joined forces to recommend a comprehensive overhaul of medical device safety, involving regulators, manufacturers, doctors and the associations themselves. The recommendations come from a joint committee of the European South Korea’s medical device market regulator, the Ministry of Food and Drug Legal Analysis: FDA 'Pet Peeves' Could Lead to Bans on Drug Companies In 2012, the US Food and Drug Administration (FDA) was granted new authority to go after Amid concerns about the risk of infections from surgical tools, federal health regulators indicate that medical device manufacturers will have to prove methods for disinfecting their products actually work. The FDA issued a final guidance on March 12 .
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