The new FLIR Research Studio is a powerful, yet simple to use software for analyzing how thermal imagery changes over time. Designed to work the way you work, the software makes thermal analysis faster, more convenient, and enables better teamwork. Whether a Windows, MacOS or Linux user, Research Studio provides customers with an easy way to quickly and efficiently display, record, and analyze accurate thermal data on their machine in any one of the available 22 languages.
FLIR offers the A6260 imaging camera for SWIR science and R&D applications. Pairing high speed performance with fully customizable features, this high-resolution detector offers improved sensitivity and linearity across the full dynamic range, making it ideal for radiometry and temperature calibrated applications.
FLIR offers the A6750 LWIR thermal imaging camera with a cooled SLS detector designed for high speed image acquisition up to 4.1 kHz with windowing. It captures all pixels simultaneously in under 190 μs for room temperature scenes, which is particularly important when monitoring fast moving objects where an uncooled thermal imaging camera would suffer from image blur.
FLIR offers the A6750 MWIR thermal imaging camera with a cooled InSb detector designed for high speed image acquisition up to 4.1 kHz. Synchronization with other instruments and events enables the capture of minute details, and available custom cold filtering options allow specific spectral detection and measurement. It is ideal for imaging through glass, measuring temperature of thin film plastics, laser profiling and detection, and optical gas imaging.
PRISYM 360 is the ONLY labeling solution dedicated to Medical Device and Life Sciences. PRISYM 360 provides organizations with complete label integrity to meet the strictest compliance requirements for FDA and EU regulations.
By focusing on the data, rather than the label/artwork, PRISYM 360 provides a revolutionary 360° outlook of your master data assets and gives the ability to control and optimize them to create a fully integrated approach across the full label lifecycle.
Due to the information being data driven, it lets you to find out where content sits quickly and easily, allowing you to deal with mass change. This feature has annually saved customers multi- million dollars on global label change, while reducing the risk of the label carrying old data or using the wrong version.
The importance of medical device labeling has increased significantly since PRISYM ID developed its first URS for a validatable enterprise labeling solution with a major global medical device manufacturer (and long-standing client) in 1999.
FLIR offers the A6700 MWIR thermal imaging camera with a cooled InSb detector designed for high speed image acquisition up to 480 Hz. Synchronization with other instruments and events enables the capture of minute details, and available custom cold filtering options allow specific spectral detection and measurement. It is ideal for imaging through glass, measuring temperature of thin film plastics, laser profiling and detection, and optical gas imaging.
Container Closure Integrity (CCI) is defined as whether the container is maintaining a sterile barrier. Intravenous (IV) bags are crucial in delivering fluids or medication quickly. Leaking parenteral packages are considered an extremely high risk as they deliver fluid directly into the bloodstream and have a high potential for microbial growth, requiring the need for sensitive and reliable CCI testing.
PTI's Seal-Scan® and Seal-Sensor® are non-contact airborne ultrasonic testing technologies. In order to use ultrasonic inspection effectively, it must be possible to place the seal in a direct line between a pair of transducers and move it (or move the transducers) along the seal. The ultrasound is transmitted and reflected at the transition from one media to the next. The greater the acoustic difference between mediums (most evident at a gas to solid transition) the more sound is reflected and the less sound transmitted through. The variation of the material thickness has only a minor effect.
Class III medical devices have a unique set of requirements and package characteristics that need a comprehensive approach to selecting the right inspection method.Advanced approaches for quality assurance of these leading-edge treatments may be needed for a variety of reasons.
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