A safer alternative to piped vacuum systems

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
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JUNE Medical launches solution for hazardous surgical plume

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
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LMT Medical Systems introduces advanced MR Diagnostics Incubator

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.
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Stryker launches industry’s first completely wireless hospital bed

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
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Fujifilm introduces Mouthpiece “B1” to prevent viral infection during peroral endoscopic procedures

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
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Anomet offers custom composite medical clad wire

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
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Hologic announces CE Mark for Faxitron Path+ specimen radiography system

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
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Siemens Healthineers introduces Biograph Vision Quadra Extended Axial FoV PET/CT scanner

Siemens Healthineers has introduced the Biograph Vision Quadra, a CE-marked positron emission tomography/computed tomography (PET/CT) scanner that is designed for clinical use as well as translational research.
In addition to the 3.2 mm silicon photomultiplier (SiPM) detector technology and Time of Flight (ToF) performance that are cornerstones of the established Biograph Vision PET/CT scanner, the Biograph Vision Quadra has an extended 106 cm axial field of view (FoV) – four times the PET axial FoV of the Biograph Vision 600. These technological features deliver significantly increased effective sensitivity and enable the clinician to image the average patient dynamically from the top of the head to the thigh in just one position. With the scanner’s extended axial FoV, the clinician can examine patient anatomy during radiopharmaceutical uptake over time. The combination of SiPM detectors and extended axial FoV permits more anatomical coverage in one bed position than a standard PET/CT scanner, enabling fast scanning at low patient radiation dose.
“The Biograph Vision Quadra is an order of magnitude more powerful than current state-of-the-art clinical scanners available today,” said James Williams, Head of the Molecular Imaging business at Siemens Healthineers. “This scanner will open possibilities for the imaging of complex and subtle biological processes that are key to the understanding of both physiology and pathophysiology alike.”
For more information, visit: www.siemens-healthineers.com/nl/molecularimaging/ pet-ct/biograph-vision-quadra
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Masimo receives FDA clearance of Rad-G Pulse Oximeter

Masimo has received FDA clearance of the Rad-G Pulse Oximeter, a rugged handheld device that provides clinically proven SET pulse oximetry, respiration rate from the pleth (RRp), and other vital parameters for both spot-checking and continuous monitoring. With its long-lasting rechargeable battery, robust rubber casing, light weight, and a convenient new direct-connect sensor capable of monitoring both adults and children, Rad-G makes it easier for clinicians to quickly assess patients and make informed decisions anywhere pulse oximetry or vital signs checking is needed. Providing the ultimate in handheld versatility, Rad-G can be used in a variety of settings, including but not limited to physicians’ offices, outpatient services, long-term care facilities, wellness clinics, first-response scenarios, and limited-resource environments.
Launching alongside the device, the new multipurpose, direct-connect Rad-G Sensor is indicated for monitoring both adult and paediatric patients. By eliminating the need to stock and carry multiple sensor types, the Rad-G Sensor further increases Rad-G’s versatility and ease of use, especially in more challenging field environments. In addition to this innovative new sensor, Rad-G is compatible with the vast portfolio of Masimo reusable and single-patient-use sensors, maximizing its flexibility and offering clinicians the ability to customize the solution based on the unique needs of each care setting.
The high-resolution screen displays a continuous pleth waveform and its fully configurable, audible alarms help alert clinicians to changes in patient status that may require their intervention.
In addition to Masimo SET oxygen saturation (SpO2), pulse rate (PR), perfusion index (Pi), and pleth variability index (PVi), Rad-G is also notable for its ability to use the same sensor to monitor respiration rate from the plethysmograph, with RRp. SpO2 and PR monitoring on Rad-G is provided using clinically proven Masimo SET Measure-through Motion and Low Perfusion pulse oximetry.
For more information, visit: www.masimo.com
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GE Healthcare introduces Serena Bright in the U.S.

GE Healthcare says its Serena Bright is now available in the United States following U.S. FDA 510(k) clearance. Serena Bright is the industry’s first contrast-enhanced guided biopsy solution allowing clinicians to conduct breast biopsy exams with contrast guidance using the same mammography equipment as that used for screening or diagnostic mammography.
Typically, for lesions found with contrastenhanced mammography and not seen on ultrasound, clinicians will use other imaging guidance, such as MRI, for biopsy procedures. Following an abnormal mammogram, it can take several weeks to get an MRI biopsy.
As the backlog of cancer screenings caused by Covid-19 persists, delays in diagnosis will likely lead to presentation at more advanced stages and poorer clinical outcomes, with one study pointing to a potential increase of 33,890 excessive cancer deaths in the U.S. alone.
Serena Bright may help decrease these delays, allowing follow-up biopsy procedures to be done in a matter of days, rather than several weeks for MRI biopsy. When compared to MRI-biopsy guided therapy, the potential benefits of Contrast Enhanced Spectral Mammography (CESM) biopsy include shortened procedure time and improved overall patient experience.
Key to this technology’s application is GE Healthcare’s SenoBright HD CESM, a diagnostic breast exam with iodine-based contrast that provides high sensitivity for more accurate breast cancer diagnosis.
By highlighting areas of unusual blood flow to localize lesions that need to be biopsied, CESM biopsy – Serena Bright – provides excellent image quality to help improve clinical confidence.
For more information, visit: www.gehealthcare.com/products/ mammography/serena-bright
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