Germany
Medizinprodukt-Marktintelligenz für Germany. Regulatorische Änderungen, Wettbewerber und Beschaffungstrends.
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A study demonstrated the equivalence of a degradable metallic device to a non-degradable device for Hallux Valgus.
A study analyzes cerebral embolization in TAVI patients using the Sentinel™ Device with different valve types.
The Erigo®Pro study evaluates a robotic tilt table's effectiveness in recovering consciousness in DOC patients.
The SeQuent® SCB study assesses its safety and efficacy in routine clinical practice per ESC guidelines.
The Idealcath by SWL Medizin GmbH is classified as a Class III medical device with UDI-DI 04251790243412.
The PRS 500 X by PROTEC X-ray Systems GmbH is registered as a Class IIb medical device in EUDAMED.
The PRS 500 X by PROTEC X-ray Systems GmbH is classified as a Class IIB medical device.
The PROVERT device by PROTEC X-ray Systems GmbH is registered as a Class I medical device in EUDAMED.
The POROUS ultrasound device is being studied for estimating bone mineral density, offering advantages over DXA.
SWL Medizin GmbH's Triones device is classified as Class III and registered in EUDAMED.
The Moritz Sitzkissen, a Class I medical device by Moritz Reha-Hilfen GmbH, is registered with UDI-DI 04255942208397.
The GermanVasc/MDEpiNet study analyzes health insurance claims to assess the safety of paclitaxel-coated devices in Germany.
The study on ticagrelor removal using CytoSorb® during surgery has been terminated.
The COVADIS pilot trial evaluates CoSeal® hydrogel's efficacy in preventing cardiac adhesions during VAD procedures.
The DIRT-study evaluates new biomarkers for diagnosing infections related to implantable cardiac devices.
A study evaluated staff acceptance of Medtronic's Vital Sync remote monitoring in intensive care settings.
A completed study validated the SelfFit app for fitting hearing aids using diagnostic audiometry.
The study comparing preoperative and postoperative visual acuity using the VirtIOL device has been terminated.
SWL Medizin GmbH's SWL-Pathfinder is a Class III medical device registered in EUDAMED.
The Rayline device by SWL Medizin GmbH is classified as Class III and has a UDI-DI of 04251790220116.