Discovery

Fabricante

376 dispositivos con un nombre similar

Más información acerca de la data acá

  • Modelo / Serial
    Affected devices may be contained in the following serial number ranges.  Model 1174: INITIAL RECALL Serial numbers 109017 thru 115660. EXPANDED RECALL serial numbers104205 thru 117464. Model 1175: INITIAL RECALL serial numbers 200731 thru 202199. EXPANDED RECALL serial numbers 200251 thru 202787 Model 1273: INITIAL RECALL serial numbers 315516 thru 324528. EXPANDED RECALL serial numbers 306216 thru 601338. Model 1274: INITIAL RECALL serial numbers 296080 thru 496546. EXPANDED RECALL serial numbers 404822 thru 498144. Model 1275: INITIAL RECALL serial numbers 500705 thru 501661. EXPANDED RECALL serial numbers 500211 thru 502015.
  • Clasificación del producto
  • Clase de dispositivo
    3
  • ¿Implante?
    Yes
  • Distribución
    worldwide. Including the United States and countries such as: Argentina, Australia, Austria, Belgium, Bolivia, Brazil, Canada, Chile, Colombia, Costa Rica, Cyprus, Czechoslovakia, Denmark, Dominican Republic, Ecuador, Egypt, Finland, France, Germany, Greece, Guadeloupe, Guyana, Hong Kong, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Lebanon, Luxembourg, Malaysia, Mexico, Netherlands, New Zealand, Norway, Panama, Peru, Poland, Polynesia, Portugal, Reunion, Russia, Saudi Arabia, Singapore,Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan ROC, Turkey, United Kingdom, Uruguay and Venezuela. EXPANDED RECALL additional countries include: China, Croatia, Korea. Lithuania, Madagascar, Maldives, Malta, Monaco, Nepal and Thailand.
  • Descripción del producto
    DISCOVERY (model nos. 1174, 1175, 1273, 1274 and 1275) pacemaker. Sterilized with gaseous ethylene oxide. Guidant Corporation , Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. DISCOVERY pacemakers are multiprogrammable pacemakers from Guidant. The family consists of both dual-chamber and single-chamber models, offering adaptive-rate therapy. DISCOVERY pacemakers use an accelerometer that allows the pacing rate to adapt to the patient's changing metabolic demand as it responds to patient activity.
  • Manufacturer
  • Modelo / Serial
    Affected devices may be contained in the following serial number ranges.  Model 481: INITIAL RECALL serial numbers 100000 thru 100115. EXPANDED RECALL serial numbers 100185, 100213, 100356, 100357, 100360. Model 981: INITIAL RECALL serial numbers 200002 thru 200041. EXPANDED RECALL serial numbers 200145, 200150, 200178, 200192, 200312. Model 1184: INITIAL RECALL serial numbers 300012 thru 300061. EXPANDED RECALL serial numbers 300159 thru 301072 and 610018 thru 610035. Model 1186: INITIAL RECALL serial numbers 500000 thru 500054. EXPANDED RECALL serial numbers 500056 thru 500444 Model 1187: INITIAL RECALL serial numbers 450000 thru 450010. EXPANDED RECALL serial numbers 450027 thru 450056. Model 1283: INITIAL RECALL serial numbers 600001 thru 600073. EXPANDED RECALL serial numbers 600214 thru 602143 Model 1284: INITIAL RECALL serial numbers 700000 thru 700079. EXPANDED RECALL serial numbers 700296, 700343, 700452, 700506, 700552, 700561, 700566. Model 1286: INITIAL RECALL serial numbers 900000 thru 900059. EXPANDED RECALL serial numbers 900045 thru 900888.
  • Clasificación del producto
  • Clase de dispositivo
    3
  • ¿Implante?
    Yes
  • Distribución
    worldwide. Including the United States and countries such as: Argentina, Australia, Austria, Belgium, Bolivia, Brazil, Canada, Chile, Colombia, Costa Rica, Cyprus, Czechoslovakia, Denmark, Dominican Republic, Ecuador, Egypt, Finland, France, Germany, Greece, Guadeloupe, Guyana, Hong Kong, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Lebanon, Luxembourg, Malaysia, Mexico, Netherlands, New Zealand, Norway, Panama, Peru, Poland, Polynesia, Portugal, Reunion, Russia, Saudi Arabia, Singapore,Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan ROC, Turkey, United Kingdom, Uruguay and Venezuela. EXPANDED RECALL additional countries include: China, Croatia, Korea. Lithuania, Madagascar, Maldives, Malta, Monaco, Nepal and Thailand.
  • Descripción del producto
    DISCOVERY II (model nos. 481, 981 1184, 1186, 1187, 1283, 1284, 1285 and 1286) pacemaker. Sterilized with gaseous ethylene oxide. Guidant . DISCOVERY II pacemakers are multiprogrammable pacemakers from Guidant. The family consists of both dual-chamber and single-chamber models, offering both adaptive-rate therapy and conventional pacing therapy. These pacemakers provide various levels of therapeutic and diagnostic functionality. DISCOVERY II adaptive-rate models have an accelerometer, which is a motion sensor that responds to patient activity.
  • Manufacturer
  • Modelo / Serial
    Model 4196-1, all units with a white electrical cord
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Nationwide, including Puerto Rico and Guam, and internationally to Canada, Mexico, Panama and Australia
  • Descripción del producto
    Wahl 2-Speed All-Body Massager with Heat and Discovery Channel brand 8-Way Massager with Heat, model 4196-1; therapeutic massager; Wahl Clipper Corporation, Sterling, IL 61081, made in China; || Please note: Wahl sells these massagers under other model numbers based on the packaging configuration. All packages contain the model 4196-1 massager, with various attachments. These package models include 4196-500, 4196-517 and 4196-519
  • Manufacturer
  • Modelo / Serial
    617243PETCT, 203688DST, ALLIANCEPETCT30, 203863DST, 973989DST, 908979DST, 212535DST, 412942DST, 814366CTPET, 202715PTCT, 443663DST, 850863FWPET, 863680DST, 251343DST, 832237EHDST, 0002584305, 574535PET, 763257DST, DMSIPCO7, EPHCPASRW1, 801408DST, 949417DST, 406255PET, 805546CT1, 415222CL1, 503692PETCT, 360SALPET, 425228DST, 402390DST1, 201996DST, AH4001PE01, 2558941, 082445040002, 082445160009, 082445160006, 082445160010, 514340DST, 423468PE01, 10495DST01, A4194408, 10094PTM70, 00060DST01, 00060DST02, A5138110, C5123618, A5215931, A99263302, A5111228, A5808512, A5279305, A5645908, YE0010, YE0009, 81DST2547033, ZWL0470, PER10934, 732292DST, ALLIANCEPCT41, DMSIPC15, 763463PC14, ALLIANCEPETCT28, ALLIANCEPETCT29, 972867DST, 082445040003, 2585577DISCPET, A5645911, YE0100, YE0113, YE0404, YE0403, 0834450002, 787269PETCT, 0002592878
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide, Worldwide. AL, CA, CT, FL, IN, MA, MD, MN, ND, NE, NJ, NY, OH, OR, PA, TN, TX, UT, WA, Puerto Rico. OUS to include: Austria, Brazil, Canada, China, Columbia, Egypt, France, Germany, Italy, Japan, Malaysia, Mexico, Netherlands, Portugal, United Kingdom, Venezuela
  • Descripción del producto
    Discovery ST PET/CT imaging system with gantry model number 5105797. Catalog Identifiers: S9114LA/LB/MA/MN, S9118LA/LB/MA/MN, S9116LA/MA. The system combines the high performance Lightspeed Plus CT with high performance PET that is optimized for routine 2D and 3D oncology, cardiology and neurology clinical studies.
  • Manufacturer
371 más