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Distributed Propulsion Concepts and Superparamagnetic Energy Harvesting Hummingbird Engine
Aerofoam
Wet Active Chevron Nozzle for Controllable Jet Noise Reduction
Magnetic Relief Valve
Active Aircraft Pylon Noise Control System
Unmanned Aerial Systems Traffic Management
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IEC 60601-1-2 Edition 4: New Requirements for Medical EMC

Plan now to ensure your medical devices comply with new IEC 60601-1-2 EMC 4th Edition standard requirements by the December 2018 effective date. Since the development cycle can be 2-3 years, it is important to understand the new standard now when designing medical devices.

Posted in: White Papers, White Papers, Electronics, Instrumentation, Bio-Medical, Medical

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Understanding Low Outgassing Adhesives

Engineers often want to know whether an adhesive is low outgassing or generic. While there are cases when nothing but a low outgassing product will do, the truth is that many so-called generic adhesives inherently have low outgassing levels. What's more, most bonding, potting, encapsulation and sealing applications don't need to meet a defined outgassing specification. Check out Master Bond’s guide to understanding when low outgassing adhesives are the right choice.

Posted in: White Papers, White Papers, Coatings & Adhesives, Materials, Medical

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Integrating Novel Materials to Improve Medical Device Performance

Today’s implantables are highly engineered assemblies with multiple complex elements that require innovative materials and sophisticated manufacturing. The development and use of new and novel materials and processes has enabled advances in both medical device performance and patient safety. Whether it’s a lighter material, a smoother surface, or a process that can be automated and repeatable, advanced technologies such as scratch-free surfaces or specialized coatings for stimulation can help extend or improve the life of implantable devices.

Posted in: White Papers, White Papers, Coatings & Adhesives, Materials, Bio-Medical, Medical, Lasers & Laser Systems, Photonics

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DIGITAL PATHOLOGY: A Primer for Microscope Camera Selection

Most pathologists today use digital systems within their practices and research projects to communicate, store data, and analyze images. Whether it’s within clinical, forensic, surgical, or other branches of pathology, communication and consultation among specialists is greatly improved by the use of digital systems and enables faster diagnosis for patients.

Posted in: White Papers, Imaging, Medical, Optics, Photonics

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Avoid the Dark Side of Quality Failure

Revealed in this eBook is a new hope that unites product lifecycle management (PLM), quality management solutions (QMS) and application lifecycle management (ALM) to enable product companies to overcome the phantom menace of global competitors and stricter compliance mandates to save the universe with great products. Your company’s team of quality experts, operation managers and engineers will learn how to embrace the power of an all-in-one product development solution.

Posted in: White Papers, White Papers, Bio-Medical, Medical

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IoT Device Battery Analysis

Explore how engineers address the consumer, industrial and medical demand for ever-longer battery life from IoT devices. Learn the tools used to provide insight into an IoT device’s complex battery consumption waveforms and how designers and manufacturers can create new ways to extend the battery life. Download Application Note.

Posted in: White Papers, White Papers, Energy Efficiency, Electronics & Computers, Bio-Medical, Medical

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Planning for Implementation of the European Union Medical Devices Regulations – Are You Prepared?

The Medical Device and In Vitro Medical Device Regulations represent the most significant change to the European legislation for medical devices for nearly 20 years. Understanding the requirements is key to your ability to develop an implementation plan to ensure continuing regulatory compliance and provide the EU market with safe medical devices.A new white paper, “Planning for Implementation of the European Union Medical Devices Regulations: Are You Prepared?” focuses on the practical aspects of implementation. It discusses decisions that need to be made and includes questions to ask about your organization’s preparedness to comply with the new requirements.Download this new white paper to learn how to address: Activities and requirements for manufacturers, authorized representatives, importers, and distributors Existing products and their technical documentation, including clinical evidence Products in the development pipeline Responsibilities of the person handling regulatory compliance, ISO 13485:2016 certification, and lifecycle management Content and maintenance of technical documentation Unique device identification, implant cards, and labelling changes PMS plans, periodic safety update reports (PSURs) or post-market surveillance reports, and post-market clinical follow-up (PMCF)

Posted in: White Papers, Manufacturing & Prototyping, Bio-Medical, FDA Compliance/Regulatory Affairs, Medical

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