Device Recall NAMIC

  • Modèle / numéro de série
    Lot Numbers: 5284422 5286610 5283649 5290525 5286542
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Recall conducted to end user level. Recall Notifications were delivered by Fed Express.
  • Description du dispositif
    Fluid Management Convenience Kits (Angioplasty Kits) intended to be used in Fluid Management || and/or Invasive Pressure Monitoring systems.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Angiodynamics Inc. (Navilyst Medical Inc.), 10 Glens Falls Tech Park, Glens Falls NY 12801-3864
  • Société-mère du fabricant (2017)
  • Source
    USFDA

66 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
    Sterile/Non-Sterile UPN Cat Num Lot Sterile Kit H749600183811 60018381 4163389;  Sterile Kit H749600308161 60030816 4155011;  Sterile Kit H749600339121 60033912 4167674;  Sterile Kit H7496005216131 60052161 4148470;  Sterile Kit H7496005216131 60052161 4152176;  Sterile Kit H7496005216131 60052161 4166769;  Sterile Kit H7496005216131 60052161 4168829;  Sterile Kit H7496005216131 60052161 4170180;  Sterile Kit H749601621861 60162186 4173288;  Sterile Kit H749601921911 60192191 4155123;  Sterile Kit H749602103071 60210307 4155130;  Sterile Kit H749602103071 60210307 4160686;  Sterile Kit H749606912341 60691234 4175188;  Sterile Kit H965600102351 60010235 4155678;  Sterile Kit H965600104921 60010492 4153182;  Sterile Kit H965600204051 60020405 4155226;  Sterile Kit H965600204051 60020405 4172242;  Sterile Kit H965600206451 60020645 4155233;  Sterile Kit H965600300681 60030068 4166803;  Sterile Kit H965600800511 60080051 4155288;  Sterile Kit H965600800511 60080051 4169451;  Sterile Kit H965601001351 60100135 4154699;  Sterile Kit H965601001351 60100135 4165389;  Sterile Kit H965601001351 60100135 4168350;  Sterile Kit H965601001351 60100135 4169879;  Sterile Kit H965601001351 60100135 4172683;  Sterile Kit H965601001351 60100135 4176389;  Sterile Kit H965602100141 60210014 4160703;  Sterile Kit H965602201531 60220153 4155363;  Sterile Kit H965PK050455S1 PK050455S 4177156;  Non-Sterile Kit H749650300641 65030064 4148480;  Non-Sterile Kit H749650300641 65030064 4168790;  Non-Sterile Kit H749650302721 64030272 4167954;  Non-Sterile Kit H749651106561 65110656 4169591;  Non-Sterile Kit H749651106561 65110656 4172687;  Non-Sterile Kit H749656900411 65690041 4166791;  Non-Sterile Kit H965650200691 65020069 4169026;  Non-Sterile Kit H965651949131 65194913 4157481;  Non-Sterile Kit H965651949131 65194913 4174714;  Non-Sterile Kit H9656522016141 652201614 4167686; Non-Sterile Kit H9656522016141 652201614 4170421;
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide) including the states of Connecticut, Florida, Illinois, Indiana, Kentucky, Maryland, Michigan, New Jersey, New York, Ohio, South Carolina, Wisconsin, Virginia and the country of Japan.
  • Description du dispositif
    NAMIC (TM) Convenience Kit --- Legal Manufacturer Navilyst Medical, Inc, 26 Forest St, Marlborough, MA 01752 USA --- Made in USA: 10 Glen Falls Technical Park, Glen Falls, NY 12801 USA --- each unit label contains the customer name under the name of the product, and each catalog number is specific to the customer. || Product usage: For use in fluid management and/or invasive pressure monitoring systems
  • Manufacturer
  • Modèle / numéro de série
    Lot 4256783, 4460497, 4575427, 4582488, 4638692, 4656910.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
  • Description du dispositif
    NAMIC Convenience Kit, LEFT HEART KIT, UPN H749602000571, REF/Catalog No. 60200057, STERILE, Rx ONLY --- For single use only. || --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
  • Manufacturer
  • Modèle / numéro de série
    Lot 4399506
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
  • Description du dispositif
    NAMIC Convenience Kit, UPN H749606204751, REF/Catalog No. 60620475, STERILE, Rx ONLY --- For single use only. --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
  • Manufacturer
  • Modèle / numéro de série
    Lot 4440346
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
  • Description du dispositif
    NAMIC Convenience Kit, LEFT HEART KIT, UPN H965600125911, REF/Catalog No. 60012591, STERILE, Rx ONLY ---For single use only. --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
  • Manufacturer
  • Modèle / numéro de série
    Lots 4600293, 4604109, 4630591, 4638147, 4643561, 4651008, 4798764, 4805945.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US Nationwide and the countries of: Canada, and Guam.
  • Description du dispositif
    NAMIC Convenience Kit, UPN H965600338021, REF/Catalog No. 60033802, STERILE, Rx ONLY ---For single use only. --- Device Listing Number D136588. || NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Systems.
  • Manufacturer
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