RheinCell Therapeutics, a developer and manufacturer of human induced pluripotent stem cells (iPSCs) as starting materials for cell therapies, has received Good Manufacturing Practice (GMP) certification and Manufacturing Authorization. This marks a landmark achievement for RheinCell, which is now among a select few iPSCs manufacturers to have received the critical certification.
Bittium, a leading specialist for secure communications, connectivity, and medical technology solutions, has released a new version of Bittium Cardiac Navigator Holter ECG Analysis Software. The new Bittium Cardiac Navigator 1.4. Software version brings improvements to the P-wave detection. This will enhance the analysis accuracy of atrial fibrillation. The new version includes also minimum and […]
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Swiss MedTech start-up Advanced Osteotomy Tools (AOT) has received CE certification for its patented CARLO® system which cuts bones precisely and contact-free with a specialized laser using a robot. CARLO stands for Cold Ablation Robot-guided Laser Osteotome.
https://interhospi.com/wp-content/uploads/sites/3/2021/02/7_AOT-SWISS.jpg28510003wmediahttps://interhospi.com/wp-content/uploads/sites/3/2020/06/Component-6-–-1.png3wmedia2021-02-26 12:24:302021-03-02 09:05:04World’s first contact-free robotic-guided laser osteotome is CE certified
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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HelpMeSee, a not-for-profit global campaign to end cataract blindness, has introduced an Eye Surgery Simulator, representing a landmark achievement in medical simulation training.
Equipped with sensory touch feedback and realistic virtual graphics, the HelpMeSee Eye Surgery Simulator, incorporated within the HelpMeSee Training Program, supports the training of cataract specialists on the Manual Small Incision Cataract Surgery (MSICS) procedure, a solution that could help end the global cataract blindness crisis.
Saro Jahani, HelpMeSee President and CEO, commented: “The HelpMeSee Eye Surgery Simulator overcomes the traditional restraints of cataract surgery training with unlimited virtual practice opportunities. It also offers the benefits of remote simulation-based training during the COVID-19 pandemic, limiting the risks of exposure to coronavirus infection.”
The HelpMeSee Eye Surgery Simulator encompasses an adaptation of an actual virtual microscope used in surgery, two haptic handpieces, a virtual syringe, the patient head and hand rest, and a touchscreen user interface, powerful visuals and simulation software, and everything required to simulate an MSICS surgery. The two handpieces and syringe represent the complete set of surgical instruments needed to perform an MSICS procedure. Programmed lessons with onscreen guides and error messages assist the student in mastering the MSICS technique and the instructor in providing objective feedback.
More than 60 million people across the world are blind or severely visually impaired simply because they cannot access cataract surgery, according to the World Health Organization (WHO) and the International Association for the Prevention of Blindness (IAPB). The HelpMeSee Simulator and training program along with partners can develop a significant number of cataract specialists that public health experts say are needed to address the developing world ophthalmologist shortage, a factor behind the cataract surgery backlog.
The simulator was the innovative vision of Flight Safety International Founder Albert L. Ueltschi and his son, James "Jim" Tyler Ueltschi. In 2010, they founded HelpMeSee to end the backlog of cataract and visual impairment cases caused by the lack of access to high-quality, affordable cataract surgery.
Jim Ueltschi, Co-Founder and Chairman of HelpMeSee, said: “This achievement will truly change the world of ophthalmology. Every specialist we train on the Eye Surgery Simulator will treat thousands of people each year. Over time, millions will have their vision restored through the cataract surgery skills honed on the HelpMeSee Simulator.”
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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Canon Medical Systems USA recently launched SOLTUS 500 Mobile Digital X-ray, giving facilities access to a portable X-ray system that is equipped with enhancements that can streamline bedside exams to help improve workflow and productivity. This will help facilities that require rapid imaging exams performed in a variety of complex situations, often at the patient’s bedside.
The FDA-cleared SOLTUS 500 has a compact design with advanced features that promote efficiency and patient safety, without compromising image quality. Features include:
Enhanced ease-of-use with intuitive tubehead controls, including an 8.4-inch (21 cm) touchscreen display and dual collimator controls for increased access and accuracy.
Increased detector wireless range and productivity with Canon Medical patented technologies. The Distributed Antenna System optimizes detector wireless range, and the Enhanced Workflow Package supports the exam from start to finish at point of care.
Exceptional safety and security features for patient, clinician and facility, including anti-collision technologies, pressure sensitive steering, improved manoeuvrability and smart ID card log-in for secure accessibility.
Simplified detector charging and storage capacity allows space and functionality for detector charging, storage and accommodating accessories such as disinfecting wipes and protective bags.
For more information, visit: us.medical.canon 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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Sony has introduced the LMD-X3200MD 32-inch medical grade LCD monitor with 4K HDR colour imaging. Its sleek design is optimized for hospital operating rooms, surgical centres and clinics.
It is designed to minimize reflected glare in brightly lit ORs, and the panel structure achieves clear, high-contrast images by controlling reflection and minimizing light dispersion in the LCD panel. This allows application of the monitor under various lighting conditions and avoids the need for ongoing adjustment of the monitor in the OR to remove potentially distracting reflections from surgical lights.
The LMD-X3200MD LCD panel and signal processing technology provide a wide colour gamut that complies with the ITU-R Recommendation BT.2020. Offering a wider colour gamut than the BT.709, colour reproduction is significantly improved with realistic visualisation. HDR technology also allows images to be produced with a wider range of brightness level, greater contrast, and rich colours. When receiving HLG (Hybrid Log-Gamma) signals from an HLG-compatible imaging system, users can simply select HLG in monitor gamma setting mode to display HDR images.
“We understand the critical importance in providing a surgeon with the highest quality image that enables greater depiction of finer anatomical structures through a simplified application,” explained Claire Bregeon, Product Marketing Manager for Healthcare at Sony Professional Solutions Europe. ‘‘With 4K resolution combined with HDR, you can see more detail in a dark body cavity and in bright areas with light reflections on membrane surfaces. If the surgeon sees better – they can perform better.”
The LMD-X3200MD also benefits from Sony’s unique A.I.M.E. (Advanced Image Multiple Enhancer) that allows you to adjust the view to enhance structure and colour for more comfortable viewing. This technology has been recently improved with new features including shadow enhancement and noise reduction. Parameters can also be set directly via the button on the front panel.
For more information, visit: www.sony.net 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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