Devices

Stryker

  • Modèle / numéro de série
    06213017, 08269017, 06230017, 08297027, 06247017, 08322017, 06257017, 08325017, 06279017, 09020017, 06306017, 09050017, 06355027, 09083017, 07025017, 09135017, 07043017, 09209017, 07067017, 09233017, 07080017, 09246017, 07114017, 09330017, 07157017, 10046017, 07172017, 10074017, 07183017, 10083017, 07197017, 10091017, 07211017, 10180017, 07220017, 10194017, 07246017, 10217017, 07282017, 10231017, 07323017, 10266017, 07356017, 10272017, 08003017, 10327027, 08017017, 10335017, 08049017, 11004017, 08064017, 11012017, 08078017, 11080017, 08141017, 11119017, 08206017, 11153017, 08248017, 11165017.
  • Classification du dispositif
    Dental Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide) and the countries of Brazil, Canada, China, Germany, Greece, Hong Kong, India, Jordan, Miramar, Saudi Arabia, Singapore, Spain, Switzerland, United Kingdom.
  • Description du dispositif
    IBO Blade, Right, for use with Stryker TPS Reciprocating Saw, REF 5100-37-901, Stryker Instruments, Kalamazoo, MI. || Product Usage: The intended use of these devices is to cut bone and hard tissue in maxillofacial procedures and have been specifically designed for osteotomies of the mandibular ramus.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation
  • 1 Event

Fabricant

Stryker Instruments Div. of Stryker Corporation
  • Adresse du fabricant
    Stryker Instruments Div. of Stryker Corporation, 4100 E Milham Ave, Portage MI 49002-9704
  • Société-mère du fabricant (2017)
    Stryker
  • Source
    USFDA

843 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

Device Recall Stryker PainPump
Device Recall Stryker PainPump
Device Recall Stryker
  • Modèle / numéro de série
    Serial numbers 0412060619, 0501073240, 0501073241, 0501073327, 0501073328, 0501073329, 0501073330, 0408062292, 0408062293, 0502069215, 0504072232, 0409062008, 0409062003, 0409062004, 0409062005, 0409062006, 0410065050, 0502069214, 0410058767, 0409062001, 0409062274, 0512070516, 0602079782, 0602079817, 0602079818, 0602079819, 0408062389, 0408062390, 0408062391, 0409062007, 0411060535, 0506071242, 0410065046, 0501073064, 0501073065, 0501073066, 0501073084, 0501073085, 0501073086, 0501073087, 0501073188, 0501073189, 0501073190, 0602079542, 0506071118, 0510071070, 0510071071, 0510071072, 0605087579, 0504072089, 0602079541, 0505069588, 0502069314, 0502069315, 0510071241, 0511071674, 0511071675, 0511071676, 0511071677, 0511071678, 0511071679, 0511071680, 0504072088, 0512070514, 0512070515, 0412060744, 0412060745, 0412060746, 0412060855, 0412060856, 0412060857, 0501073001, 0501073002, 0501073003, 0502069148, 0601084043, 0507070537, 0510071069, 0502069034, 0502069035, 0502069036, 0502069150, 0502069151, 0502069152, 0502069153, 0510071243, 0410058765, 0507070691, 0507070692, 0507070693, 0507070694, 0507070695, 0507070696, 0507070697, 0507070698, 0507070699, 0507070700, 0603084573, 0409062002, 0410058766, 0502069149, 0503068501, 0503068502, 0503068503, 0506071116, 0506071117, 0506071241, 0603084574, 0410065049, 0501073373, 0501073374, 0501073375, 0501073376, 0502069032, 0502069033, 0502069313, 0603084672, 0411060618, 0411060619, 0411060620, 0411060621, 0411060802, 0411060803, 0411060804, 0412060504, 0412060505, 0412060506, 0412060616, 0412060617, 0412060618, 0505069589, 0505069590, 0505069591, 0505069592, 0410065047, 0509069501, 0509069502, 0505069749, 0505069750, 0502069216,  0410065045, 0410065048, 0411060801, 0408062151, 0409062273, 0409062275, 0502069312, 0503068633, 0503068634, 0503068635, 0503068636, 0511071540, 0511071541, 0511071542, 0511071543 and 0503068637.
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide (including USA, Australia, Canada, England, Germany, Italy, Romania and Singapore).
  • Description du dispositif
    Stryker Trio Mobile Surgery Platform; Model 1033.
  • Manufacturer
    Stryker Medical Div. of Stryker Corporation
Device Recall Stryker
  • Modèle / numéro de série
    Lots 04051142--06121FE2, 04051142--06123FE2
  • Classification du dispositif
    Obstetrical and Gynecological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide
  • Description du dispositif
    Stryker brand Insufflation Tube Set and High Flow Insufflation Tube Set, || Model Numbers: || 620-030-201, || 620-030-301
  • Manufacturer
    Stryker Endoscopy
Device Recall Stryker PowerPRO
  • Modèle / numéro de série
    All units with a serial number lower than 060739380. (units manufactured between 1 Oct 2005 and 15 July 2006)
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution ---- including USA and countries of Canada, China, Germany and Switzerland.
  • Description du dispositif
    Stryker Power-PRO Powered Ambulance Cot, Model 6500.
  • Manufacturer
    Stryker Medical Div. of Stryker Corporation
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