Devices

Device Recall AXIOM Sireskop SD

  • Modèle / numéro de série
    Serial numbers: 51010, 71136, 51007, 51008, 71019, 71080, 71172, 71067, 41012, 71015, 71038, 71102, 71104, 71169, 51006, 51011, 51024, 51028, 71026, 71039, 71083, 71117, 71119, 41027, 71120, 71121, 41028, 71137, 71138, 71149, 71158, 71161, 71167, 71168, 71170, 51060, 71160, 51026, 71030, 71059, 71033, 71037, 41006, 51052, 51064, 71001, 71082, 71114, 71141, 71148, 71152, 71156, 51046, 71181, 51013, 51044, 71075, 71098, 51054, 71020, 71021, 71074, 71088, 41026, 71135, 71140, 71055, 71006, 71017, 71042, 71073, 71162, 71174, 41003, 51049, 71053, 71128, 71131, 41022, 71096, 71099, 71129, 51009, 51036, 51045, 71069, 71087, 71144, 41008, 71014, 71016, 71028, 71109, 71130, 71004, 71051, 71090, 71157, 51029, 51030, 51069, 71009, 71011, 71034, 71035, 71126, 71127, 71145, 51003, 51016, 71022, 71029, 71164, 51043, 51070, 71061, 71064, 71110, 71116, 51001, 51057, 41014, 71124, 71133, 51012, 51050, 71070, 71142, 71095, 41011, 51047, 71023, 71076, 71081, 71084, 51041, 41010, 71032, 41029, 71002, 71065, 71105, 71115, 51005, 71068, 51017, 51018, 51023, 71043, 71046, 41020, 71091, 71092, 71101, 71108, 71139, 71146, 71150, 71155, 71178, 51015, 51059, 51066, 71013, 71057, 71062, 71097, 41013, 71024, 41023, 71086, 51037, 71010, 71106, 71112, 51065, 51068, 71008, 41017, 71078, 41024, 71079, 71111, 71018, 71147, 51002, 71040, 41002, 51019, 51020, 41005, 51033, 41007, 51040, 51048, 51051, 51055, 51061, 71003, 71007, 71012, 41018, 71025, 41019, 71045, 71063, 71100, 71103, 71113, 71122, 71125, 71153, 71154, 71159, 71163, 71171, 71173, 71177, 51004, 51021, 51025, 51058, 71048. 71058, 71060, 71072, 41001, 51022, 51031, 51035, 51039, 71027, 71175, 51063, 71005, 71066, 71089, 71165, 71166, 71123, 71151, and 51056.
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    AXIOM Sireskop SD Model numbers 8890415 and 8890407. The product is intended for use as radiographic and fluoroscopic imaging device.
  • Manufacturer
    Siemens Medical Solutions USA, Inc
  • 1 Event

Fabricant

Siemens Medical Solutions USA, Inc
  • Adresse du fabricant
    Siemens Medical Solutions USA, Inc, 51 Valley Stream Pkwy, Malvern PA 19355
  • Société-mère du fabricant (2017)
    Siemens Ag
  • Source
    USFDA

Un dispositif médical avec un nom similaire

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Device Recall AXIOM SIRESKOP SD, SIRESKOP SX, AXIOM LUMINOS
  • Modèle / numéro de série
    Model Numbers: 3111668, 3111676, 8890407, 8890415, and 10093902
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution including AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, and WY.
  • Description du dispositif
    AXIOM SIRESKOP SD, SIRESKOP SX, AXIOM LUMINOS || System, X-Ray, Fluoroscopic, image-intensified; solid state x-ray imager (flat panel/digital imager)
  • Manufacturer
    Siemens Medical Solutions USA, Inc