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Ce Marked Medical Device Articles & Analysis

12 news found

TannerMedico A/S awarded AAA-rating – expanding global distribution network for Asonor®

TannerMedico A/S awarded AAA-rating – expanding global distribution network for Asonor®

As the manufacturer of Asonor®, a CE-marked Class IIa medical device for the treatment of snoring, we offer a well-documented product with: 20+ years of clinical experience Documented effect Approved and registered in more than 70 countries We are now expanding our global distributor network. ...

ByTannerMedico A/S - Asonor


CardioWise™ Receives ISO 13485:2016 Clearance for Design, Development, and Marketing of Software as a Medical Device (SaMD) For the Medical Device Industry

CardioWise™ Receives ISO 13485:2016 Clearance for Design, Development, and Marketing of Software as a Medical Device (SaMD) For the Medical Device Industry

Perry Johnson Registrars Certificate C2022-02910 was issued July 16, 2022, and represents the first step in the process of obtaining a CE mark and Medical Device Registration for the European Union (EU) that will allow CardioWise to market its products there. ...

ByCardioWise Inc.


New Bone Data Comparing ImpediMed’s SOZO to DXA in Cancer Patients to be Presented at 39th Annual Miami Breast Cancer Conference

New Bone Data Comparing ImpediMed’s SOZO to DXA in Cancer Patients to be Presented at 39th Annual Miami Breast Cancer Conference

Developing new indications creates opportunity to expand SOZO utilization by placing additional SOZO devices and adding new licenses to existing devices. New indications also support the strategy for building large corporate accounts, many of which have interest in co-development and regulatory clearance for new ways to use SOZO to benefit their cancer patients ...

ByImpediMed Inc.


New Data Show Statistically Significant Reduction in Chronic Cancer-Related Lymphedema with Early Detection Using ImpediMed’s L-Dex® Technology and Intervention

New Data Show Statistically Significant Reduction in Chronic Cancer-Related Lymphedema with Early Detection Using ImpediMed’s L-Dex® Technology and Intervention

Frank Vicini, ImpediMed’s Chief Medical Officer. “Many of these patients have survived surgery, chemotherapy, radiation and other treatments, only to face a long-term, painful battle with lymphedema. ...

ByImpediMed Inc.


The American Academy of Orthopedic Surgeons has just recognized that when integrated in patient education, Knee Kinesiography with the KneeKG system provides statistically significant and clinically superior improvements compared to the results obtained w

The American Academy of Orthopedic Surgeons has just recognized that when integrated in patient education, Knee Kinesiography with the KneeKG system provides statistically significant and clinically superior improvements compared to the results obtained w

Michael Suk, Professor of Orthopaedic Surgery and Chair of the Musculoskeletal Institute at Geisinger Health System in Danville, PA, Orthopaedic Surgeon, and American Medical Association Board of Trustee. “Tools that can support healthcare providers identifying biomechanical dysfunctions and quantifying the cause of pain and symptoms is a new frontier in diagnosing and ...

ByEmovi


EDGe Surgical Receives CE Mark Certification for EDG Ortho 65mm Electronic Depth Gauge

EDGe Surgical Receives CE Mark Certification for EDG Ortho 65mm Electronic Depth Gauge

EDGe Surgical, Inc., a company focused on developing and manufacturing smart orthopedic and spine surgical instruments, announced today that it has received a CE Certificate of Conformity from its notified body permitting CE mark of the company’s EDG Ortho 65mm single-use electronic depth gauge in the European Union market. ...

ByEDGe Surgical, Inc.


Medical certification obtained for the products of the Vaud startup

Medical certification obtained for the products of the Vaud startup

SteriLux passes the course of medical certification for the European market, thus demonstrating that its technology meets the most demanding standards in the field of health. Sterilizing heat-sensitive medical instruments without chemicals: this is the objective that the Vaud-based startup SteriLux has set itself since its creation in 2014. ...

BySteriLux SA


Oncomfort and Vygon sign international partnership for commercialization of Sedakit™, the Digital Sedation™ Virtual Reality solution

Oncomfort and Vygon sign international partnership for commercialization of Sedakit™, the Digital Sedation™ Virtual Reality solution

Oncomfort, the Belgian inventor of Digital SedationTM - a new method for relieving patients’ pain and anxiety without medication –, and Vygon, global group specializing in single-use medical devices, today announce their commercial partnership in six European countries. The strong synergy between Vygon's specialization and ...

ByOncomfort


Liberate Medical Announces CE Marking for its VentFree Respiratory Muscle Stimulator

Liberate Medical Announces CE Marking for its VentFree Respiratory Muscle Stimulator

Liberate Medical, a medical device company developing novel non-invasive electrical muscle stimulation devices to help patients with pulmonary conditions, today announced that it has received CE marking for its VentFree™ Respiratory Muscle Stimulator and ISO 13485 certification for its ...

ByLiberate Medical, LLC


Epihunter awarded $200k grant to support the commercialization of its AI seizure detection algorithm

Epihunter awarded $200k grant to support the commercialization of its AI seizure detection algorithm

“Boston Children’s Hospital’s clinicians and researchers have extensive experience in setting up and running medical device studies, including those involving seizure monitors. We are eager to measure epihunter’s impact on therapy decision making and daily life,” Rotenberg adds. ...

ByEpihunter NV


Belgian healthtech startup, epihunter, launches second breakthrough for absence epilepsy

Belgian healthtech startup, epihunter, launches second breakthrough for absence epilepsy

Belgian startup, epihunter, introduces automated video functionality to their CE-marked seizure detection app - a breakthrough for children and adults with epilepsy, their families and doctors. ...

ByEpihunter NV


Waters ACQUITY UPLC I-Class/Xevo TQ-S micro System available as a U.S. FDA Class I, CE-Marked Medical Device

Waters ACQUITY UPLC I-Class/Xevo TQ-S micro System available as a U.S. FDA Class I, CE-Marked Medical Device

Waters Corporation (NYSE: WAT) today announced that the Waters® ACQUITY UPLC® I-Class IVD/Xevo® TQ-S micro IVD System is now manufactured as a U.S. FDA Class I medical device and is CE Marked to the European Directive 98/79/EC (IVDD). ...

ByWaters Corporation

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