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. . Sur BFM Business, le directeur général de la société française annonce que son cœur artificiel entre désormais dans une phase industrielle.
. . (CercleFinance. com) - bioMérieux annonce le renforcement de sa gamme Argène pour identifier le SRAS-CoV-2, qui peut désormais être utilisé, en complément des prélèvements nasopharyngés, sur des prélèvements salivaires et pharyngés pour détecter le virus responsable de Covid-19
The company expects the CE mark to improve the accessibility of personal devices to become more easily available 3D printed CMF titanium implant from Materialize 10, 2020 (GLOBE NEWSWIRE) - Materialize NV (Nasdaq: MTLS), a leader in 3D technology solutions in the industrial and medical markets, announced that it has received CE Marking for most orthopedic and maxillofacial (CMF) procedures. 3D printed anatomical models, surgical guides and patient compatible implants, MATRIALIZ is a leading and world leader in personalized solutions, helping patients and surgeons on six continents produce more than 350The company became one of the first companies to obtain this kind of certification for a wide range of 3D printed medical devices This certification will make technology more accessible to surgeons CE approval indicates that the medical device meets the requirements of the European Medical Devices Directive So far, Materialise's custom devices have benefited from The specially designed procedure, which requires a prescription for each device This procedure guarantees the quality of the devices and the safety of the patients, but brings administrative obstacles to the production in greater quantities “When the European Medical Devices Directive was issued in 1993, the use of personal devices was exceptional in the past 30 years, we developed the planning And 3D printing to extend this technology to a much larger audience at Materialize, we're talking about thousands of devices being delivered around the world each year.Personal devices are no longer the exception This CE marking certification demonstrates that these personal devices meet the same stringent quality requirements as regular devices. , Despite the challenges involved in making each device match the specific anatomy of a patient, ”she says Well Brigitte De Witt, Vice President and Managing Director of Matrials Medic, Materialize has a legacy of adhering to the highest possible safety standards and is one of the first companies to have a complete personal portfolio CE certified. The company believes that this type of certification will help raise the bar in the industry to ensure safety. Patients and transparency in personal device production The CE marking will also improve accessibility to make personal devices more easily available With the implementation of the new process, surgeons will not need to sign a prescription for the devices they request, which means less paperwork and more flexibility for pharmacists who manage personal devices within the hospital. “The advantage of using dedicated devices is that it adds more predictability in the surgical setting and allows to treat any clinical condition, including the most difficult cases Now, obtaining this CE mark for our larger business portfolio will help in providing these personal devices to a greater number of patients, removing Some administrative limitations for our clients, ”Brigitte adds. Since its founding in 1990, custom solutions have been the core business of a company Realize Medical begins with customization with planning, the launch of Mimics software in 1992 enabled precision engineering based on 3D images, which formed the basis for the advanced digital planning solutions available today. Materialize was also the first company to introduce custom 3D printing solutions in the operating room with the launch of surgical knee guides In 2007 the launch of the personal CMF implant in 2009 introduced a design breakthrough with a porous structure of titanium that allowed rebuilding of lost bone fragments This CE certification is another milestone in achieving higher quality standards in personalized medicine Although the CE marking is a European concept, the system Widely accepted as proof of compliance in other markets This certification joins other CE marks that Materialize has already obtained on medical software solutions, such as Mimics Innovation Suite and Mimics Enlight on Materialize that integrates more than three decades of 3D printing experience into a range of solutions The software and 3D printing services, which together form the backbone of the 3D printing industry, enable open and flexible Materialise solutions Players in a wide range of industries, including healthcare, automotive, aerospace, art and design, and consumer goods, from creating innovative 3D printing applications aiming to make the world a better and healthier place. Materiales is headquartered in Belgium, with branches around the world, and brings together Among the largest group of software developers in the industry and one of the largest 3D printing facilities in the world For additional information, please visit: www verified com L-101478-01 Attachments * MaterialiseCMFimplant * Femur_01 Contact: Bram Smits Embodiment Press @ Tjsdcom
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