The penumbra cat8 indigo system (cat8) was kinked approximately 4. There was partial improvement of flow, but total occlusion remained. Do not use the INDIGO Aspiration System with a pump other than the Penumbra Aspiration Pump. Mechanical thrombectomy was performed. Tareq Kass-Hout. These pages are not intended for patients or for members of the general public. The Penumbra IndigoSystem Separatoris intended for use with our Indigo Systems CATfamily of catheters to enable the removal of a wide range of thrombus. Use the INDIGO Aspiration System in conjunction with fluoroscopic visualization. Separator 8, 150 cm Length, 0.072 in. The sustained aspiration power provided by the Penumbra ENGINE allowed rapid TIMI 3 flow restoration and removal of the distal emboli. Excessive aspiration or failure to close the INDIGO Aspiration Tubing valve when aspiration is complete is not recommended.
After IVUS, the stent was dilated to 3.75 mm. Lightning Aspiration Tubing has dual pressure sensors for real-time blood flow monitoring. Distal emboli causing PDA occlusion after manual aspiration. The Indigo System CAT3, CAT5, CAT6, CAT8 and CATD ?are engineered to be robust, durable, and trackable for use in the peripheral anatomy. Warnings/Precautions The canister is intended for single use only. Unrestrained torquing or forced insertion of the catheter or separator against resistance may result in damage to the device or vessel. Penumbra Aspiration Pump: Since the initial launch of the Indigo System, catheter technology as well as techniques have advanced. Initial experience with a mechanical aspiration catheter for thrombus removal during percutaneous intervention: a multicenter retrospective case series. In-Date Home; 3M KCI; Abbott; Acist; Acumed; Acutus; AD Surgical; Adhezion; Aesculap; Alcon Mechanical power aspiration with the Indigo System CAT RX (Penumbra, Inc.), introduced in 2018, continues to gain in popularity as a solution for high thrombus burden in the coronaries. The Indigo Separator 4 is not intended for use as a guidewire. Possible complications include, but are not limited to, the following: Contraindications The CAT family of catheters is the foundation of Penumbra's Indigo system. These pages are not intended for patients or for members of the general public.
Penumbra CAT8XTORQ115 CAT8 Indigo System Aspiration Catheter 8F(x) Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 12 inches (30 cm) to any part of LIGHTNING Aspiration Tubing. The INDIGO SEPARATOR is not intended for use as a guidewire. left-arrow The pulmonary capillary wedge pressure is 10 mmHg. Remove and service the PENUMBRA ENGINE if liquids or solids have been drawn into the PENUMBRA ENGINE.
MAUDE Adverse Event Report: PENUMBRA, INC. INDIGO SYSTEM ASPIRATION 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.
Penumbra Cat 8 - IndiaMART The Indigo System CAT3, CAT5, CAT6, CAT8 and CATD ?are engineered to be robust, durable, and trackable for use in the peripheral anatomy. She was in a rehab facility prior to this new event recovering from her CVA.
Neuro | Penumbra, Inc. | Mechanical Thrombectomy & Embolization Catheters - Aspiration Catheters - Page 1 - Medical Materials If the cause cannot be determined, withdraw the device or system as a unit. Precautions The device is intended for single use only. If repositioning of the INDIGO Aspiration Catheter is necessary during the revascularization procedure, such repositioning should be performed over an appropriate guidewire using standard catheter and guidewire techniques. The CAT family of catheters is the foundation of Penumbra's Indigo System. Use prior to the Use By date.
Indigo System | Penumbra Inc The Indigo System and CAT8 - Endovascular Today Available in a selection of sizes, the CAT family can provide access to distal peripheral vessels of the upper and lower extremities, including below the knee. The initial angiogram confirmed an occlusion with extensive thrombus burden of a dominant left circumflex artery and TIMI 0 flow (Figure 1). Excessive aspiration or failure to close the Indigo Aspiration Tubing valve when aspiration is complete is not recommended. Only use replacement fuse with correct rating (see Table 1 for fuse rating). INDIGO Aspiration Catheters and Separators: As part of the INDIGO Aspiration System, the INDIGO Aspiration Catheters and Separators are indicated for the removal of fresh, soft emboli and thrombi from vessels of the peripheral arterial and venous systems, and for the treatment of pulmonary embolism. Potential Adverse Events INDIGO Aspiration Tubing: Saint Louis, Missouri
The Indigo Aspiration System should only be used by physicians who have received appropriate training in interventional techniques. Penumbras IndigoAspiration System can be used to remove emboli and thrombi from vessels of the peripheral arterial and venous systems, and for treatment of pulmonary embolism. Figure 2. Figure 3. Do not use open or damaged packages. Tip directionality for circumferential aspiration, Live feedback during procedure with integrated clot catcher, Penumbra ENGINE is capable of delivering and maintaining nearly pure vacuum (-29 inHg or 98.2 kPa) with the disposablePenumbra ENGINE Canister. Equipment is not safe for MR use. The catheters (CAT3, CAT RX*, CAT5, CAT6, CAT8, CATD) vary in diameters from 3.4 to 8 F and lengths of 50 to 150 cm to . The INDIGO Aspiration System is intended for the removal of fresh, soft emboli and thrombi from vessels of the peripheral arterial and venous systems and certain central circulatory system conditions such as pulmonary emboli using continuous aspiration. The Penumbra Aspiration Pump is indicated as a vacuum source for Penumbra Aspiration Systems. The Penumbra P logos, 3D, 3D Revascularization Device, ACE, BENCHMARK, CAT, Indigo, LANTERN, MAX, Neuron, Neuron MAX, Penumbra ENGINE, Penumbra JET, Penumbra System, Penumbra SMART COIL, POD, Ruby, Separator, Velocity, and WAVE are registered trademarks or trademarks of Penumbra, Inc. in the USA and other countries. Most recently, Penumbra launched Lightning Intelligent Aspiration which enables physicians to focus on optimizing thrombus removal using the system's unique clot detection mechanism. Indigo Aspiration System (CAT RX and Separator 4)- Penumbra Engine Pump and Canister. The complaint indicated that the cat8 was kinked during the procedure. Available in a selection of sizes, the CAT family can provide access to distal peripheral vessels of the upper and lower extremities, including below the knee. gus.theodos@bjc.org; @gtheodosmd
Penumbra Aspiration Pump The Penumbra Aspiration Pump is indicated as a vacuum source for Penumbra Aspiration Systems. Download scientific diagram | A, Penumbra Indigo System Continuous Aspiration Mechanical Thrombectomy Catheter (CAT8). After one pass with mechanical thrombectomy using CAT RX, the thrombus was removed and flow was restored to the pedal arch via the plantar posterior tibial artery (Figure 2 and Figure 3).
Penumbra CAT8TORQ85 CAT8 Indigo Aspiration Catheter 8, TORQ tip, 85cm The Indigo Aspiration System is intended for the removal of fresh, soft emboli and thrombi from vessels of the peripheral arterial and venous systems and certain central circulatory system conditions such as pulmonary emboli using continuous aspiration. The CAT family of catheters is the foundation of Penumbras Indigo System. Distal OD, Sterile, Single-Use, Disposable, For CAT8 Penumbra Devices, Indigo Aspiration Catheters, Removal of Fresh, Soft Emboli and Thrombi from Vessels of Peripheral Arterial and Venous Systems Figure 1.
Indigo System CAT RX | Penumbra Inc To avoid risk of electrical shock, this equipment must only be connected to a supply mains with protective earth.
Penumbra System Products - Medical Materials Suhail Dohad, MD, FACC
Penumbra's LANTERN Delivery Microcatheter integrates a highly trackable 2.6 F microcatheter with a high-flow lumen to facilitate confident delivery of Ruby Coil, POD, and Packing Coil even in tortuous anatomy. Unrestrained torquing or forced insertion of the catheter or SEPARATOR against resistance may result in damage to the device or vessel. CAT7 and CAT12 are the next generation of the Indigo System Catheters. Potential Adverse Events Possible complications include, but are not limited to, the following: 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; hemorrhage; ischemia; kidney damage from contrast media; neurological deficits including stroke; vessel spasm, thrombosis, dissection, or perforation; intimal disruption; myocardial infarction; emergent surgery; fibrillation; hypotension; respiratory failure; peripheral thromboembolic events. Order Qty. As part of the Indigo Aspiration System, the Indigo CAT RX Aspiration Catheters and Indigo Separator 4 are indicated for the removal of fresh, soft emboli and thrombi from vessels in the coronary and peripheral vasculature. Mechanical power aspiration with a continuous vacuum source and large lumen aspiration catheter was first introduced in the neurovascular space when Penumbra revolutionized thrombus removal for acute ischemic stroke patients. indicated to connect the INDIGO CAT RX Aspiration Catheters to the Penumbra Aspiration Pump. Further evaluation of the returned device revealed kinks in the catheter shaft. Power aspiration with CAT RX has allowed us to successfully remove thrombus in patients presenting with acute coronary syndrome, establishing quick distal reperfusion and also visualization of the underlying stenosis. The patient was brought back to the cardiac cath lab for follow-up angiography that revealed TIMI 0 flow of the RCA (Figure 1). Return all damaged devices and packaging to the manufacturer/distributor. The Indigo System met its efficacy and safety endpoints by reducing right-to-left ventricle (RV/LV) ratio at 48 hours by 27.3% (mean ratio reduction, 0.43; 95% confidence interval, 0.380.47; P < .0001) and had a low major adverse event of 1.7% (2/119). Potential Adverse Events Prior to use, please refer to the Instructions for Use for complete product indications, contraindications, warnings, precautions, potential adverse events, and detailed instructions for use. The Indigo System utilizes the Penumbra ENGINEaspiration source capable of delivering nearly pure, continuous vacuum (-29 inHg or 98.2 kPa) to our catheters, enabling thrombus removal in vessels of various sizes. Use of LIGHTNING Aspiration Tubing adjacent to other equipment should be avoided because it could result in improper operation.
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