Germany
Medizinprodukt-Marktintelligenz für Germany. Regulatorische Änderungen, Wettbewerber und Beschaffungstrends.
Neueste Signale
The Nit-Occlud® Lê VSD Spiral Coil System is evaluated for safety and effectiveness in VSD treatment across multiple countries.
The completed study assessed the LynxPatch's feasibility for pre-operative cardiac risk assessment.
AiM Medical Robotics will integrate its robotic neurosurgery platform with Siemens' MRI systems.
The PROMISE registry is recruiting to assess safety and effectiveness of percutaneous cannulation in minimally-invasive heart valve surgery.
A study evaluates outcomes of BIOTRONIK dual-chamber pacemakers with LBBAP and CLS for atrial fibrillation reduction.
Study shows LAA occluder implantation affects ANP and BNP levels in atrial fibrillation patients.
The FlexStent system has been evaluated for efficacy and safety in treating femoral artery disease in 100 patients in Germany.
Dr. Manuel Martina will discuss advancements in printed circuit board technology for medical electronics at Med-Tech Expo 2026.
GPE MedTech Systeme GmbH has registered a medical device with the FDA under product code GCX.
MEDNOSBRO GmbH has registered one medical device with the FDA under product code GAD.
Almikro GmbH & Co. KG has registered a medical device with product code HET.
TimeWaver Production GmbH has registered two medical devices with the FDA under product code IPF.
Moritz Reha-Hilfen GmbH registered the Moritz Keilkissen as a Class I medical device in EUDAMED.
The Moritz Keilkissen, a Class I medical device by Moritz Reha-Hilfen GmbH, is registered with UDI-DI 04255942207345.
The Moritz Keilkissen by Moritz Reha-Hilfen GmbH is registered as a Class I medical device with UDI-DI 04255942204658.
The Moritz Keilkissen, a Class I medical device by Moritz Reha-Hilfen GmbH, is registered with UDI-DI 04255942201053.
The Moritz Keilkissen, a Class I medical device by Moritz Reha-Hilfen GmbH, has UDI-DI 04255942202937.
The Moritz Keilkissen, a Class I medical device, is registered under UDI-DI 04260727756840 by Moritz Reha-Hilfen GmbH.
The Moritz Keilkissen, a Class I medical device, is registered by Moritz Reha-Hilfen GmbH with UDI-DI 04255942203064.
The PROSLIDE 32 B System by PROTEC X-ray Systems GmbH is classified as Class IIB and registered with UDI-DI 04260502642542.