Hologic has received CE Mark for the Faxitron Path+ specimen radiography system, the latest addition to the Company’s growing portfolio of digital specimen radiography solutions.
The Faxitron Path+ system features a superior, high-resolution imaging detector which enables pathologists to image a wide range of specimens of varying sizes, including bone, foetal remains and breast tissue directly in the lab. By combining a larger field of view with intuitive, easy-to-use software, the system provides pathologists with accurate results in an efficient manner. Additionally, the clear specimen images produced enable pathologists to satisfy the regulatory demands for De-Calcification End Point testing.
The Faxitron Path+ system provides up to 10x geometric magnification, enabling imaging of small microcalcifications and ensuring accurate diagnoses. Optimal X-ray exposure settings can be selected regardless of specimen makeup and density to ensure the highest image quality is maintained. These features offer pathologists more versatile imaging options and help to reduce the Turn Around Time (TAT) for reports.
For more information, visit: www.hologic.com Read more
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US-based Anomet is offering a custom composite medical clad wire that can combine up to three different materials for use with CRM, neurostimulation, vascular, and related devices.
By using different materials the medical clad wire can meet specific design requirements, performance, and cost criteria; especially where solid wire is limited. Typical configurations for implantable devices include: Platinum-iridium clad tantalum, Platinum clad MP35N®, Silver cored MP35N®, 316LVM clad tantalum, Nitinol clad platinum, and Gold clad nitinol.
Anomet’s medical clad wire is ideally suited for meeting design criteria for corrosion resistance, wear resistance, contact resistance, biocompatibility, radiopacity, strength, conductivity, solderability, formability and more.
The medical clad wire has a smooth consistent finish and can be made in sizes from 0.050 mm to 3.175 mm O.D. with 2% or more cladding thickness.
Anomet Medical Clad Wire is priced according to configuration and quantity. Samples and price quotations are available upon request.
For more information, visit: www.anometproducts.com Read more
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Fujifilm has launched the Mouthpiece “B1” developed to catch and reduce the droplets emitted by the patient during endoscopic examination of the upper gastrointestinal tract. The device helps to minimize the risk to healthcare workers and fellow patients from becoming infected with Covid-19 and various other pathogens.
The Mouthpiece “B1”, which incorporates a sponge rubber, a droplet reduction accessory and a drape shield, is placed in the patient’s mouth and fixed with a headband.
The accessory is easy to handle and does not inconvenience the patient when compared to using a standard mouthpiece. The accessory can be used with different types of endoscopes with various diameters, ensuring that there are no gaps between the endoscope and the mouthpiece.
The drape shield covers the patient’s face and shields healthcare workers from patients during peroral endoscopy, thereby reducing the risk of viral infection by way of droplet transmission.
It reduces the spread of aerosol droplets by incorporating sponges which have slits in the insertion part of the mouthpiece where the endoscope is introduced, this design ensures that there are no gaps between the endoscope and the mouthpiece.
The mouthpiece is designed with extra depth to create space between the face shield and the patient’s face to maximize air ventilation for the patient. It also reduces discomfort caused by covering the face with the shield.
For more information, visit: www.fujifilm.eu Read more
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Stryker has launched globally the industry’s first completely wireless hospital bed, ProCuity. This intelligent bed was designed to help reduce in-hospital patient falls at all acuity levels, improve nurse workflow efficiencies and safety, as well as help lower hospital costs. It is the only bed on the market that can connect seamlessly to nurse call systems without the use of cables or wires.
“Patient safety is at the foundation of everything we do at Stryker,” said Jessica Mathieson, VP/GM of Acute Care, Stryker. “Leveraging our long history in innovation, ProCuity is the culmination of years of extensive research and feedback from nurses and other healthcare professionals to create what is truly a ‘brilliance in a bed’ solution. It was designed to improve patient outcomes and assist caregivers for years to come.”
Set at an industry low height of 11.5 inches (29.2 cm), ProCuity is ergonomically designed with the latest technologies to promote safe patient handling and help reduce fall-related injuries, including intuitive patient positioning and bed alarms as well as ergonomic side rails. Helping to address nurse call cable connectivity issues, ProCuity can be equipped with fully wireless features. Additionally, the bed’s easy-to-use touchscreens and other key components makes the job of caregivers easier and more efficient, while providing for a more enhanced patient experience.
Specific key features of ProCuity include: Completely Wireless: ProCuity’s Secure Connect wireless solution makes it the only bed on the market that can connect without cables to nurse call systems. Additionally, with iBed Wireless, all bed data, including bed config-uration and exit alarm activity, are wirelessly compatible with facilities’ hospital information systems. To help give caregivers increased visibility to safe bed configuration and bed exit alarm activity, ProCuity can also integrate with Stryker’s optional patient-centric clinical dashboard, iBed Vision. Ergonomic Side Rails: Three-position Secure Assist side rails allow for easier patient entry and exit as well as nurse-patient interaction. Intuitive Patient and Bed Monitoring Systems: ProCuity’s exclusive Adaptive Bed Alarm uses load cell technology to sense a patient’s weight and will alert nurses if a patient is out of position or has left the bed. With ProCuity’s iBed Watch system, all operational aspects of the bed, from side rail positioning, head of bed angle and height, are monitored to ensure that it is always in a safe position for the patient. Caregivers are alerted immediately if any components are out of position. Zoom Motorized Drive: To help caregivers move patients safely and more efficiently, ProCuity Z and ZM models come complete with Zoom Motorized Drive, a motorcycle throttle-like touch handle that deploys the central fifth wheel. It also comes with one-touch electric brakes. Standard, Customizable Platform: From MedSurg units to the ICU, the ProCuity bed series is designed to meet all patient acuity levels. This helps make standardization across hospitals easier, while reducing hospital costs associated with renting specialty beds and the need for bed transfers and extra staff. Enhanced Patient Experience: To provide greater flexibility for taller patients, ProCuity has an integrated bed extender, which allows the bed to stretch an additional 12 inches (30.5 cm) in length. It also comes with a USB port and holder to allow patients to charge and store personal electronic devices like phones. Guarantee Program: Through Stryker’s Financial Guarantee program, the company promises customers will see a 50% reduction in bed-related falls occurring on Stryker beds utilizing iBed Wireless technology (terms and conditions apply).
For more information, visit: www.stryker.com/us/en/acute-care/ products/procuity Read more
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LMT Medical Systems is where MRI meets Neonatology; the MR Diagnostics Incubator System nomag® IC ADVANCED allows newborns and premature babies to be transported directly from the NICU into the MR suite for examination by optimal, non-invasive Magnetic Resonance Imaging. The baby is protected inside the life sustaining, temperature and humidity controlled MR-incubator throughout the entire transport and MRI examination.
In the new generation, the MR Diagnostics Incubator System nomag®IC ADVANCED, LMT Medical Systems GmbH has brought functionality many steps forward. Patient access and noise protection in the MR scanner were improved.
There is a wider patient bed and the overall weight of the incubator is reduced.
The nomag®IC ADVANCED is compatible with the devices of the leading MRI manufacturers. It can be easily attached to the corresponding MRI devices. The functional reliability has been officially tested and approved. Read more
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JUNE Medical has launched the eVeck Colposcopy Plume Evacuation Kit for the safe and efficient removal of surgical plume. Surgical plume is an unavoidable result of interventional procedures where diathermy, electrosurgery, laser and ultrasonic devices cut into tissue. It can release an unpleasant odour but, more importantly, can contain toxic, infectious or carcinogenic material – such as hydrogen peroxide gas, HPV or SARS-CoV-2 – that could be hazardous to theatre staff or indeed the patient. As a result, exposure to surgical plume has been linked to eye, nose and throat irritation, nausea, headaches, coughs, nasal congestion, asthma, and asthma-like symptoms.
The single use eVeck Kit comes ready assembled, with an integrated HEPA pre filter, a flexi connector that fits assorted speculum models, and tubing that links to a plume evacuation system and is reinforced to prevent crushing and kinking.
Renowned electro surgery consultant Steve Veck has worked on the project, advising medical device specialist Mosaic Surgical. He said: “Surgical plume is an inevitable consequence of procedures that use electrosurgical techniques, and there is clear evidence showing the dangers it presents to personnel. Despite this, the most efficient removal methods are not mandatory in every territory, or for every case. The eVeck eliminates this issue by attaching directly to the speculum, positioning it close to the surgical site to clear all the damaging materials before staff and patients can be exposed to them.”
Angela Spang, CEO of JUNE Medical, commented: “We are delighted to be able to offer this simple but vital solution that can prevent surgical teams from being exposed to the hazards of surgical plume. We hope that more widespread use of the eVeck Kit will have a significant long-term effect on improving the health of healthcare professionals.”
For more information, visit: junemedical.co.uk/eveck Read more
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Medela Healthcare mobile suction devices – a safer alternative to wall vacuum – can help expand critical care capacity and support UK hospitals in the fight against COVID-19.
Used worldwide, the company’s portable medical suction machines are designed to provide crucial suction and fluid removal during respiratory treatment provided with ventilators.
Traditionally, hospitals ensure a patient’s airway is clear by utilising suction that relies on central wall piped vacuum. However, guidance published by the National Health Service advises hospitals against using piped vacuum to support infectious disease units to reduce the risk of virus spread and cross-contamination.
A previous study looking at contamination rates for wall-mounted suction units discovered contamination on over 30% of devices. Hence, portable medical suction machines are recommended for COVID-19 care. Medela offers a range of portable suction pumps which are available with a virus filter capable of reducing cross-contamination from COVID-19 with filtration efficiency of greater than 99.9%.
These compact devices offer flexibility to hospitals while reducing the risk of viral transmission. When used with disposable collection systems, portable suction machines reduce staff exposure to hazardous fluids, while devices equipped with virus filters further reduce risk of cross-contamination and viral exposure to staff.
Standard of care in the ICU requires each patient to be provided with a single suction device, which helps to decrease the risk of lung infections, prolonged hypoxia, and pooling of secretions in the lung.
For more information, visit: https://covid19. medelahealthcare.com/solutions Read more
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Biotronik has introduced a new injectable cardiac monitor (ICM). The BIOMONITOR IIIm is equipped with a unique algorithm that significantly reduces false positive atrial fibrillation (AF) detections due to ectopic beats.
Physicians can lose time reviewing these nonactionable episodes. Research shows that 52% of false positive AF episodes occur due to premature ectopic beats, which can be falsely detected as AF.
According to Biotronik, the new device can achieve a 72% reduction in false positives while maintaining 100% of AF-related sensitivity. It removes single ectopic beats out of the AF detection algorithm, enhancing diagnostic accuracy. This will make physicians’ workload more efficient.
These new features are supported by image quality comparable to those recorded on a gold-standard 12-lead ECG.
BIOMONITOR IIIm is also the industry leader in battery longevity with 5.5 years of continuous service, providing long-term post-ablation or cryptogenic stroke monitoring. It is also backed by the Patient App, which allows patients to include vital symptom data, providing physicians with symptom-rhythm correlation which strengthens diagnostic precision.
For more information, visit: www.biotronik.com/en-de/products/arrhythmiamonitoring/ biomonitorIIIm Read more
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Materials scientists from Nanyang Technological University, Singapore have invented a new type of surgical glue that can bond blood vessels and close wounds, even when their surfaces are wet.
Named CaproGlu, it is activated by a low dose of ultraviolet light that cures it in seconds, turning it from a liquid glue into a solid but flexible biorubber – a biocompatible material that can be resorbed by the tissue after a few weeks.
Unlike current bio-adhesives – which need two chemicals to be mixed prior to use – the CaproGlu is a one-pot liquid gel solution that comes ready-to-use.
In a study published in Biomaterials in July they showed in animal experiments that blood vessels can be rejoined with just four stitches and a mesh wrapper dipped in CaproGlu, compared to the usual eight stitches that are required for a reliable and unobstructed join. The authors estimate that this will reduce surgery time by 25 per cent, as surgeons spend less time and effort stitching up blood vessels and tissues.
They also showed that CaproGlu can also be used to deliver local anaesthetics or pain relief medication to tissues in the body, which may be useful both during and post operation.
The adhesion strength of CaproGlu was compared to other commercial bioadhesives on the market and was found to be three to seven times stronger, and is on a par with the shear strength of collagen and muscle tissue found in the human body.
CaproGlu combines two ingredients into a single-component formulation that does not require additives. The first is polycaprolactone – a biodegradable polymer which has been approved by the United States Food and Drug Administration for specific applications used in the human body – and the second: diazirine, a light-sensitive molecule that can form strong bonds when activated.
The research team have filed for a provisional patent for the biorubber glue. Read more
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Philips has introduced OmniWire, the world’s first solid core pressure wire for coronary artery interventional procedures.
Its breakthrough solid core construction enables physicians to more easily manoeuvre the wire in the patient’s circulatory system to measure blood pressure along the vessel and guide the delivery of catheters and stents.
The new wire supports iFR (instant wave-Free Ratio) measurements, the only resting index supported by randomized controlled outcome trials, as well as FFR (fractional flow reserve) measurements. It also integrates with the Philips IntraSight interventional applications platform, which can co-register iFR data onto the angiogram to precisely identify the parts of vessels requiring treatment.
Traditional pressure wires use a hollow metal tube (hypotube) to house the wiring that transmits the pressure information. Due to their thin walls, these wires can be challenging to manoeuvre and can sometimes kink, potentially becoming damaged during the procedure. OmniWire is the world’s first solid core pressure guidewire, using advanced conductive ribbons embedded in its outer polymer layer to communicate pressure information. The distal part of the wire is made from Nitinol, a super-elastic, durable material that is commonly used in non-diagnostic, interventional ‘workhorse’ guide wires. The proximal part of the wire is constructed from a highstrength cobalt alloy that provides the high durability required for complex and multi-vessel cases.
Commenting on the device, Dr. Jasvindar Singh, director of the catheterization lab at Barnes Jewish Hospital and associate professor at Washington University in St. Louis, U.S., who performed the first human case with OmniWire in the United States, said: “I have been very impressed with the handling of OmniWire, the new solid core design performed beautifully, and I was able to navigate the difficult case easily. We used iFR co-registration and found that the patient needed a stent. I was then able to perform the whole procedure working over OmniWire. This is truly an innovation in percutaneous coronary interventions.”
OmniWire has received clearance from the U.S. FDA and approval from the Japan Pharmaceuticals and Medical Devices Agency. Read more
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