Devices

Medtronic

  • Modelo / Serial
    Lot Numbers: 0000001696 0000005659 0000009476 0000042018 0000044719 0000045231 0000064050 0000068017 0000068397 0000082398 0000084406 0000085999 0000095233 0000104293 0000104342 0000115247 0000123723 0000125309 0000138086 0000150459 0000169173 0000176133 176535 186865 201667 204626 205350 211785 213371 214942 220436
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Foreign: Austria, Australia, Bahrain, Bulgaria, Canada, Czech Republic, Denmark, Germany, Hungary, Italy, Jordan, France, Greece, Japan, Hong Kong, India, Italy, Norway, Poland, Portugal, Saudi Arabia, Spain, Sweden, Switzerland, UK.
  • Descripción del producto
    CATH. GUIDE 6F SR3.5 LAUNCHER || CATHETER LA6SR35 LA 6F 100CM SR35 Coronary Guiding catheter designed to provide a pathway through which therapeutic and/or diagnostic devices are introduced into the coronary or peripheral vascular system. || Product Number: LA6SR35
  • Manufacturer
    Medtronic, Inc.
  • 1 Event

Fabricante

Medtronic, Inc.
  • Dirección del fabricante
    Medtronic, Inc., 35 -37A Cherry Hill Dr, Danvers MA 01923-2565
  • Source
    USFDA

829 dispositivos con un nombre similar

Más información acerca de la data acá

Device Recall Medtronic GRAFTON (R) DBM, Flex 2.5cm x 10cm, REF T42100
  • Modelo / Serial
    A16707-098, A16707-099, A16707-100, A16707-101, A16707-102, A16707-103, A16707-104, A16707-105, A16707-106, A16707-107, A16707-108, A16707-109, A16707-110, A16707-111, A16707-112, A16707-113, A16707-114, A16707-115, A16707-116, A16707-117, A16707-118, A16707-119, A16707-120, A16707-121, A16707-122, A16707-123, A16707-124, A16707-125, A16707-142, and A16707-147
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    US Distribution in the states of: MO, FL, MN, OH, MI, TX, and NJ.
  • Descripción del producto
    Medtronic GRAFTON (R) DBM, Flex 2.5cm x 10cm, REF T42100, Rx only, STERILE A, QTY: 1 EA, Medtronic Sofamor Danek, USA, Inc., 1800 Pyramid Place, Memphis, TN 38132 || Orthopaedic - filler, bone void
  • Manufacturer
    Medtronic Sofamor Danek USA Inc
Device Recall Medtronic Oarm Imaging System
  • Modelo / Serial
    Model No. BI-700-00027 and BI-700-00028 Serial number range: 00102 through 00753 and B13080721, B13080722, B13090729, B13120763, B13120764, B13120766, B13120768, B13120769
  • Clasificación del producto
    Radiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    USA (nationwide) Distribution
  • Descripción del producto
    Medtronic O-arm Imaging System Mobile X-ray system. || Model No. BI-700-00027 and BI-700-00028 || The 0-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits from 2D and 3D information of anatomic structures and objects with high x-ray attenuation such as bony anatomy and metallic objects. The 0-ann Imaging System is compatible with certain Image Guided Surgery Systems.
  • Manufacturer
    Medtronic Navigation, Inc.
Device Recall Medtronic Select 3D Arterial Cannula
  • Modelo / Serial
    Model 78618, Lot numbers: 2011041199, 2011062306, 2011100971, 2011102092,  2011120307, 2012051764, 2012061644, 2012080274, 2012110107, 2012120373,  2013010071, 2013050197, 2013081170, 2013102358, 201203C853.   Model 78620, Lot numbers: 2011030255, 2011040939, 2011041341, 2011101160 2011111043, 2012011041, 2012020540, 2012070617, 2012110017, 2012111257,  2013031297, 2013050408, 2013060024, 2013060816, 2013070896, 2013090420,  2013091570, 2013101359.   Model 78718, Lot numbers: 2011020219, 2011051461, 2011051501, 2011060279,  2011081265, 2011091551, 2011100022, 2011111305, 2012011048, 2012032171,  2012040645, 2012070832, 2012071313, 2013031493, 2013041737, 2013051367,  2013060409, 2013091960, 2013102157, 2013110588, 201110C116, 201203C855.   Model 78720, Lot numbers: 2011010067, 2011021825, 2011062606, 2011062607,  2011070536, 2011071117, 2011080605, 2011081029, 2011081501, 2011082463,  2011090046, 2011090047, 2011100092, 2012011142, 2012011424, 2012051863,  2012060210, 2012061344, 2012061868, 2012120133, 2012120781, 2012120941,  2012121072, 2013030331, 2013030943, 2013080633, 2013081206, 2013110894,  2013120553.
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution: US (Nationwide) including Puerto Rico, and Internationally to: Algeria, Argentina, Austria, Belgium, Bosnia And Herzegovina, Brazil, Canada, Cyprus, El Salvador, France, Georgia, Germany, Greece, Hungary, India, Ireland, Italy, Japan, Jordan, Kuwait, Netherlands, Oman, Paraguay, Poland, Portugal, Russian Federation, Saudi Arabia, Slovakia, Spain, Sweden, Switzerland, Thailand, Turkey, United Kingdom, Venezuela, and Yemen.
  • Descripción del producto
    Medtronic Select 3D Arterial Cannulae. Vented, models 78618 (18 Fr.) and 78620 (20 Fr.). Non-Vented Cannulae, models 78718 (18 Fr.) and 78720 (20 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. || The Select 3D Arterial Cannulae both have clear flexible, thin wall wire-wound PVC bodies with angled, beveled tips. The proximal end of the cannula includes a 3/8" (0.95 cm) vented or non-vented connector with a peel cap. The vented connector allows air to be vented from the cannula before connection to the perfusion line. || The Select 3D Arterial Cannula tip has three integrated flutes which help diffuse and disperse blood flow. The cannula body features a tip orientation line indicating direction of the cannula tip during cannulation. Overall cannula length is 11.5" (29.2 cm). || These cannulae are intended for use in perfusion of the ascending aorta during short term (6 hours or less) cardiopulmonary bypass.
  • Manufacturer
    Medtronic Inc. Cardiac Rhythm Disease Management
Device Recall Medtronic Select 3D Arterial Cannula
  • Modelo / Serial
    Model 78622, Lot numbers: 2011031714, 2011040345, 2011050373, 2011060471,  2011060641, 2011060642, 2011070099, 2011072408, 2011081502, 2011102965,  2011111215, 2011120575, 2012011143, 2012011425, 2012020052, 2012040536,  2012051387, 2012090216, 2012101333 ,2013010957, 2013011791, 2013020303,  2013030729, 2013040209, 2013040282, 2013040710, 2013041272, 2013051447,  2013060736, 2013071836, 2013072009, 201105C105, 201203C854.   Model 78722, Lot numbers: 2011031588, 2011031885, 2011051006, 2011051226,  2011061585, 2011071672, 2011082216, 2011091825 , 2011101670, 2011102093,  2011110717, 2011120059, 2012060478, 2012061056, 2012061057, 2012061725,  2012070570, 2012090657, 2013011121, 2013021260, 2013030685, 2013040494,  2013040595, 2013070162, 2013070483, 2013081289, 2013081603, 201108C227.
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution: US (Nationwide) including Puerto Rico, and Internationally to: Algeria, Argentina, Austria, Belgium, Bosnia And Herzegovina, Brazil, Canada, Cyprus, El Salvador, France, Georgia, Germany, Greece, Hungary, India, Ireland, Italy, Japan, Jordan, Kuwait, Netherlands, Oman, Paraguay, Poland, Portugal, Russian Federation, Saudi Arabia, Slovakia, Spain, Sweden, Switzerland, Thailand, Turkey, United Kingdom, Venezuela, and Yemen.
  • Descripción del producto
    Medtronic Select 3D Arterial Cannulae. Vented, model 78622 (22 Fr.). Non-Vented Cannulae, model 78722 (22 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. || The Cannula consists of a curved, angled or beveled tip with or without flange that is permanently attached to a molded, clear, flexible PVC tapered body or wirebound PVC body. The cannula body features a tip orientation line to indicate direction of the cannula tip during cannulation. The proximal end of the cannula includes a connection site or a molded 0.95 cm (3/8 in) barbed connector with or without a molded plastic vent plug or peel cap. The vent plug or peel cap allows air to be vented from the cannula before connection to the perfusion line. || These cannulae are intended for use in perfusion of the ascending aorta during short term (6 hours or less) cardiopulmonary bypass.
  • Manufacturer
    Medtronic Inc. Cardiac Rhythm Disease Management
Device Recall Medtronic Select 3D Arterial Cannula
  • Modelo / Serial
    Model 78624, Lot numbers: 2011010432, 2011010514, 2011010515, 2011011141,  2011011543, 2011021907, 2011040344, 2011040946, 2011060613, 2011060865,  2011070535, 2011071749, 2011081635, 2011110330, 2011120304, 2011120305,  2011121133, 2012060424, 2012060431, 2012070886, 2012080324, 2012081353,  2012081928, 2012090013, 2012120521, 2012121021, 2012121414, 2013031142,  2013050555, 2013050805, 2013051225, 2013051640, 2013060249, 2013090499,  2013090570, 2013091332, 2013091924, 201106C140, 201203C844, 201310C579.   Model 78724, Lot numbers: 2011032145, 2011050718, 2011060852, 2011092067,  2011102225, 2012032345, 2012071614, 2012081704, 2012081973, 2013031364,  2013051818, 2013060581, 2013070831, 2013080858, 2013100654, 2013110548,  2014010275, 201108C228, 201203C842.
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution: US (Nationwide) including Puerto Rico, and Internationally to: Algeria, Argentina, Austria, Belgium, Bosnia And Herzegovina, Brazil, Canada, Cyprus, El Salvador, France, Georgia, Germany, Greece, Hungary, India, Ireland, Italy, Japan, Jordan, Kuwait, Netherlands, Oman, Paraguay, Poland, Portugal, Russian Federation, Saudi Arabia, Slovakia, Spain, Sweden, Switzerland, Thailand, Turkey, United Kingdom, Venezuela, and Yemen.
  • Descripción del producto
    Medtronic Select 3D Arterial Cannulae. Vented, model 78624 (24 Fr.). Non-Vented Cannulae, model 78724 (24 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. || The Cannula consists of a curved, angled or beveled tip with or without flange that is permanently attached to a molded, clear, flexible PVC tapered body or wirebound PVC body. The cannula body features a tip orientation line to indicate direction of the cannula tip during cannulation. The proximal end of the cannula includes a connection site or a molded 0.95 cm (3/8 in) barbed connector with or without a molded plastic vent plug or peel cap. The vent plug or peel cap allows air to be vented from the cannula before connection to the perfusion line. || These cannulae are intended for use in perfusion of the ascending aorta during short term (6 hours or less) cardiopulmonary bypass.
  • Manufacturer
    Medtronic Inc. Cardiac Rhythm Disease Management
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