BMJ Case Rep. 2015, 2015:011782. The PubMed wordmark and PubMed logo are registered trademarks of the U.S. Department of Health and Human Services (HHS). Inspira aspiration catheters are designed to access the targeted vessels to restore cerebral blood flow and retrieve clots in patients experiencing acute ischemic stroke (AIS) due to a large vessel occlusion (LVO) Infinity aspiration catheters approved in EU. Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the Penumbra ENGINE. As part of the Penumbra System, the Penumbra Sterile Aspiration Tubing is indicated to connect the Penumbra Reperfusion Catheters to the Penumbra Aspiration Pump. government site. Indications for use:The Q Aspiration Catheter is indicated for use in the removal of fresh, soft emboli and thrombi in the peripheral and neurovascular systems. Nasopharyngeal airway - Wikipedia Refining Access Introducing the Monopoint Reperfusion System The Inspira aspiration catheters represent the first neurovascular device to receive approval under the new European MDR CE certification process. Learn more and transmitted securely. Refer to the Reperfusion Catheter labeling for dimensional information. Do not reuse. In recent years, however, the treatments of cerebral infarction and aneurysm alike are evolving rapidly to use catheters in what is called "neurovascular . allergic reaction and anaphylaxis from contrast media; acute occlusion; air embolism; arteriovenous fistula; death; device malfunction; distal embolization; emboli; false aneurysm formation; hematoma or hemorrhage at access site; inability to completely remove thrombus; infection; intracranial hemorrhage; ischemia; kidney damage from contrast media; neurological deficits including stroke; vessel spasm, thrombosis, dissection, or perforation; radiation exposure that may lead to cataracts, skin reddening, burns, alopecia, or neoplasia from x-ray exposure. We aimed to characterize different catheters' aspiration performance on stiff clots in an in vitro vascular model. With excellent trackability and 2X the aspiration force, Q is the choice for small vessels. The Penumbra JET D is designed to navigate smaller, distal vessels and extract clot efficiently with the power of the Penumbra ENGINE aspiration source. Esperance 5F & 6F Aspiration Catheter obtained FDA 510(k) clearance. Administration of anticoagulants and antiplatelets should be suspended until 24 hours post-treatment. Nurs Stand. The NeuronTMGuide catheter (Penumbra, Inc. Alameda, CA, USA) was placed distally at the carotid siphon to obtain maximum support for use of the mechanical stroke devices. There are no known contraindications. If repositioning of the Penumbra Reperfusion Catheter is necessary during the revascularization procedure, such repositioning should be performed over an appropriate neurovascular guidewire using standard microcatheter and guidewire techniques. The Q Aspiration Catheter* is uniquely designed to deliver up to 2x greater flow rates to maximize clot removal in even the most challenging vessels. We evaluated the performance of a novel aspiration catheter system designed to maximize lumen size, and compare it to other commercially available aspiration catheters. Access and Delivery Products for Neurovascular Treatment The workhorse Providing smooth tracking, stable delivery and a versatile platform, the Excelsior XT-17 Microcatheter is designed to be your go-to microcatheter. Medical management and acute post stroke care should follow the ASA guidelines.1 Any neurological deterioration should be evaluated by urgent CT scan and other evaluations as indicated according to investigator/hospital best practice. Reactcatheter features an unique COil + BRAid design that provides the perfect balance between navigability and durability. Do not use open or damaged packages.