Medtronic

  • Modelo / Serial
    Lot Numbers: 0000009532 0000013672 0000019809 0000022777 0000044800 0000045282 0000050729 0000056338 0000075247 0000076693 0000083944 0000096010 0000107906 0000123126 0000132923 175760 178292 180185 181735 182416 182417 183000 188007 203620 206606 212408 213693 219667
  • Clasificación del producto
  • 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 7F SR4.0 LAUNCHER || CATHETER LA7SR40 LA 7F 100CM SR40 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: LA7SR40
  • Manufacturer
  • 2 Events

Fabricante

  • 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

  • Modelo / Serial
    Serial Numbers: 109R, 118R, 124, 136, 159 ,170, 218, 222, 223, 236, 239 , 299, 309R, 402, 410, 412, 414.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA, including the states of AL, CO, FL, IA, MI, IA, NC, NE, NY and the countries of South Africa, Italy, and Spain.
  • Descripción del producto
    Medtronic O-arm¿ Imaging System. Product Numbers: BI-700-00027-100, BI-700-00027-100R, BI-700-00027-120, BI-700-00027-120R, BI-700-00027-230, BI-700-00027-230R.
  • Manufacturer
  • Modelo / Serial
  • Descripción del producto
    Spinal implants - locking nuts used in the Medtronic Colorado II spinal implant system. Catalogue number 8634111. Lots: W07G2386, W07G2387, W07G2388, W07G2389, W07G2751, W07H0440, W07H1809 and W07H1810.
  • Manufacturer
  • Modelo / Serial
    Lot number 120203.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution--US (nationwide) including the states of CA, FL, MA, LA, and MI and the countries of Switzerland, Saudi Arabia, Lebanon, Canada and Korea.
  • Descripción del producto
    The Vertex Max Drill Tube is a component within the Navigated Vertex Max Drill Guide Set (item 9733370). The Navigated Vertex Max Drill Guide Set is intended to be used with a Medtronic Computer Assisted Surgery System to help assist with screw placement during spine surgical procedures. The device is reusable and requires sterilization according to product labeling. || .
  • Manufacturer
  • Modelo / Serial
    Pack Model Pack Lot 0E27R16- 11239917  11252800  11264666; 1A30R6- 12132577  12219267; 2493R24- 11187015  11199707  11224309  11227205  11556735; 2493R25- 11646941  11713200  11745242  11813334  11852673  11886412  11990393  12033630  12114699  12178107  12191642  12450856; 5D56R5- 11298229  11357085  11465358  11541270  11601193  11654853  11702415  11745232  11766305  11822320  11838721  11852677  11930380  12024708  12166379  12292156; 5Z93R4- 11713132  11736880  11749958  11766283  11808651  11860604  11878689  11911068  11948473 5Z93R5- 12236493;  12411746 7E64R2- 11933798; 7J53R2- 12172725; 7M13R1- 12168157; 7M14R1- 12349772; 7N16R- 12349786; 7P25R1- 12327801  12449801  12457250; 7P93R1- 12349795  12374420; 7Q11R1- 12344028  12456303; BB7L63R2- 12408737; BB7N26R- 12312571; CB5174R11- 11293051  11315344  11334856  11489271  11745162  11886341  11977682  12019852  12062713  12098852  12139621  12146752  12258941  12277502  12326468  12421465  206110946;  CB5175R13- 11292866  11334859  11432873  11442937  12182778  12411655;  CB5Q03R6- 11713162  11766245  11787583  11923139  11934952;  CB5Q03R7- 12114626; CB6C53R6- 12423767; CB7C15R2- 12411647; CB7C59R2- 11731501;  11813316  11838743  11869767  11908794  11982413  12019907  12146796  12151706  12201727  12292133  12423702; CB7C60R2- 11687047  11724030  11843434  11878672; CB7C74R2- 11895167; CB7D91R5- 11961280  12130493  12146882  12191604  12277455  12411687  12423760;  CB7E35R2- 11839101;  CB7E38R1- 11843886  11885844  11990360  12105025  12133083  12159400;  CB7G21R4- 12032413  12033728  12040524  12083359  12360622;  CB7L48R1- 12301694; CB7L72R1- 12155258; CB7P82R1- 12440601; HY6U96R2- 206133995; HY6Y52R2- 11826276; HY7E87R1- 11830948  11898103  11923498  12323794  12435409; SS7J91R3- 12175428; SSCB7L48R- 12120109; SSTL7G78R1 -11986264; TL5S33R7- 12093478;  12139612  12172589  12315375;  TL6V77R1- 11217931  11260111;  TL7B51R1- 11559097  11622968  11664762  11687063  11712834;  TL7G20R3- 12258680  12271138  12360554 TL7G78R3- 12067309; TL7R87R1- 206114578  206145379
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution--USA (nationwide) including the states of AZ, CA, CT, FL, GA, IL IA, MD, MA, MI, MS, NJ, NY, OH, OK, SC, TN, TX and WI. and the countries of CANADA and MALAYSIA.
  • Descripción del producto
    Medtronic Intersept Custom Tubing Pack with or without coating ( Carmeda BioActive Surfact, Carmeda BioActive Surfact and Trillium Biosurface,or Balance Biosurface) with the following Model numbers: || 0E27R16, 1A30R6, 2493R24, 2493R25, 5D56R5, 5Z93R4, 5Z93R5, 7E64R2, 7J53R2, 7M13R1, 7M14R1, 7N16R, 7P25R1, 7P93R1, 7Q11R1, BB7L63R2, BB7N26R, CB5174R11, CB175R13, CB5Q03R6, CB5Q03R7, CB6C53R6, CB7C15R2, CB7C59R2, CB7C60R2, CB7C74R2, CB7D91R5, CB7E35R2, CB7E38R1, CB7G21R4, CB7L48R1, CB7L72R1, CB7P82R1, HY6U96R2, HY6Y52R2, HY7E87R1, SS7J91R3, SSCB7L48R, SSTL7G78R1,TL5S33R7, TL6VTTR1, TL7B51R1, TL7G20R3, TL7G78R3, TL7R87R1. || Sterilized Using Ethylene Oxide, Nonpyrogenic, Assembled in Mexico, Manufacturer Medtronic, Inc, Minneapolis, Mn 55432 || Product is used by perfusionists as part of the extracorporeal circuit during cardiopulmonary bypass procedures, and is configured specifically as designated by each customer.
  • Manufacturer
  • Modelo / Serial
    Product Catalog Numbers: 9732719, 9732719R, 9733346, 9733346R, BI-700-00027, BI-700-00027R, BI-700-00027-GER, BI-700-00027-GERR, BI-700-00027-100, BI-700-00027-100R, BI-700-00027-120, BI-700-00027-120R, BI-700-00027-230, BI-700-00027-230R  Units with serial numbers 101 through 564 and unit 580 are affected. Serial numbers 565 and higher are not affected .
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution - USA Nationwide and the countries of: Canada, AUSTRIA, BELGIUM, BRAZIL, BULGARIA, CHILE, CHINA, CROATIA, CZECH REPUBLIC, DENMARK,FINLAND, FRANCE, GERMANY, GREECE, INDIA, IRELAND, ISRAEL, ITALY, JAPAN ,KOREA, REPUBLIC OF KUWAIT, LEBANON, LIBYAN ARAB JAMAHIRIYA, MEXICO, NETHERLANDS, New Zealand, POLAND, RUSSIAN FEDERATION, SAUDI ARABIA, SINGAPORE, SLOVAKIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, Taiwan(R.O.C.) , THAILAND, TURKEY, UNITED ARAB EMIRATES. and UNITED KINGDOM.
  • Descripción del producto
    Medtronic O-arm Imaging System || Product Usage: || image-intensified fluoroscopic x-ray system, mobile
  • Manufacturer
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