Professionisti del settore sanitario
Adult Extracorporeal Circuit Cannuale
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Si, sono un operatore sanitario
Note: Ai sensi e per gli effetti dell’Art. 76 D.P.R. 445/2000 consapevole della responsabilità e delle conseguenze civili e penali previste in caso di dichiarazioni mendaci e/o formazione od uso di atti falsi, nonché in caso di esibizione atti contenenti dati non più corrispondenti a verità e consapevole altresì che qualora emerga la non veridicità del contenuto della presente decadranno i benefici per i quali la stessa è rilasciata confermo di essere un OPERATORE SANITARIO.
I contenuti presenti in questo sito contengono informazioni rivolte agli operatori sanitari, in quanto si riferiscono a prodotti rientranti nella categoria dei dispositivi medici che richiedono l’impiego o l’intervento da parte di professionisti del settore medico-sanitario.
Professionisti del settore sanitario
Contraindication: This device is not intended for use except as indicated. This cannula is contraindicated for use in procedures where the chambers of the heart will be opened or in cases with septal defects.
Indication: This cannula is intended for use in venous drainage via the right atrium and inferior vena cava simultaneously during cardiopulmonary bypass surgery up to six hours or less.
Warning: The introduction of air into the right heart may result in the immediate total loss of venous drainage to the extracorporeal circulation.
Caution: Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Caution: Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgery procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a listing of indications, contraindications, precautions, warnings, and potential adverse events, please refer to the Instructions for Use.
®*Third party brands are trademarks of their respective owners. All other brands are trademarks of a Medtronic company. Soft-Flow arterial cannulae are manufactured by MC3, Inc. and exclusively distributed by Medtronic.
Contraindication: This device is not intended for use except as indicated.
Indication: This product is intended for use with cardiopulmonary bypass as an arterial return cannula.
Warning: The introduction of air into the right heart may result in the immediate total loss of venous drainage to the extracorporeal circulation.
Caution: Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use
Contraindication: This device is not intended for use except as indicated.
Indication: This product is intended for use with cardiopulmonary bypass as an arterial return cannula.
Warning: For EOPA models with Dilator Tip Introducer, a guidewire must be used for proper placement of introducer tip while inserting cannula to avoid trauma to the back wall of the aorta.
Use imaging to ensure that guidewire is properly positioned in the descending arch of the aorta.
Caution: Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Contraindication: This device is not intended for use except as indicated.
Indication: These cannulae are intended for use in perfusion of the ascending aorta during short term (6 hours or less) cardiopulmonary bypass.
Warning: Avoid pointing the cannula tip directly toward the branch arteries of the aortic arch to minimize the possibility of directing any dislodged emboli into the arteries or causing increased blood pressure in the brain. Avoid directing the tip at the aortic valve.
Cannula tip must be inserted beyond side ports to minimum depth marks to avoid possibility of tissue dissection of the aorta.
Do not exceed maximum recommended flow rates.
Caution: Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Important Safety Information:
Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac procedures.
For a listing of indications, contraindications, precautions, warnings and potential adverse events, please refer to the Instructions for Use. Caution: Federal law (USA) restricts this device to or on the order of a physician.
Contraindication: This device is not intended for use except as indicated.
Indication: The MiAR™ cannula is intended for use during cardiopulmonary bypass for the delivery of cardioplegia Antegrade through the Aorta for up to six hours.
Caution: Additional care and caution may be necessary due to the unique adaptations required for minimally invasive techniques Care should be taken when inserting the needle to prevent perforation of the back wall of the aorta.
Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Contraindication: This device is not intended for use except as indicated.
Indication: For use in cardiopulmonary bypass surgery for delivering cardioplegia solutions, venting the left heart through the aortic root and aspiration of air from the aorta.
Caution: Care should be taken when inserting the needle to prevent perforation of the back wall of the aorta.
Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Contraindication: This device is not intended for use except as indicated.
Indication: The cannula is intended for use during cardiopulmonary bypass surgery for the delivery of cardioplegia retrogradely through the coronary sinus.
Caution: Extreme caution should be exercised while introducing the cannula into the coronary sinus. Do not over inflate the balloon. Do not force the cannula into the coronary sinus as this may cause vessel damage.
Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Contraindication: This device is not intended for use except as indicated.
Indication: This adapter is intended for use in conjunction with cardiopulmonary bypass surgery.
Caution: Use the lowest possible pressure to reduce risk of hemolysis or risk of vessel damage.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Contraindication: This device is not intended for use except as indicated.
Indication: The cannula is intended for use during cardiopulmonary bypass surgery for the delivery of cardioplegia retrogradely through the coronary sinus.
Caution: Extreme caution should be exercised while introducing the cannula into the coronary sinus. Do not over inflate the balloon. Do not force the cannula into the coronary sinus as this may cause vessel damage.
Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Contraindication: This device is not intended for use except as indicated.
Indication: This adapter is intended for use in conjunction with cardiopulmonary bypass surgery.
Caution: Use the lowest possible pressure to reduce risk of hemolysis or risk of vessel damage.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Contraindication: The Pericardial Sump (#12010, #12011) is not intended to be placed through a valve to drain a closed cardiac chamber. This device is not intended for use except as indicated.
Indication: These sumps are intended for draining the pericardial sac. The Intracardiac Sump can also be used to drain the cardiac chambers.
Caution: Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Contraindication: This device is not intended for use except as indicated.
Warning: Care and caution should be taken to avoid damage to vessels and cardiac tissue during cannulation or other cardiac surgical procedures.
Caution: Federal law (USA) restricts this device to sale by or on the order of a physician. For a complete listing of indications, contraindications, precautions and warnings, please refer to the Instructions for Use.
Medtronic Italia S.p.A. Società a socio unico soggetta ad attività di direzione e coordinamento da parte di Medtronic PLC.
Cap. soc. € 1.200.487,00 - Codice fiscale, partita IVA e numero di iscrizione al Registro delle Imprese di Milano-Monza-Brianza-Lodi 09238800156 – REA MI – 1275682. Sede Legale e Uffici Via Varesina, 162 Edificio Raimondi - 20156 Milano.