Devices

Device Recall Arterial Line Kit

  • Modèle / numéro de série
    Material number ASK-04510-MM3
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution
  • Description du dispositif
    Arterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions || The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
  • Manufacturer
    Arrow International Inc
  • 1 Event

Fabricant

Arrow International Inc
  • Adresse du fabricant
    Arrow International Inc, 2400 Bernville Rd, Reading PA 19605-9607
  • Société-mère du fabricant (2017)
    Teleflex Incorporated
  • Source
    USFDA

7 dispositifs médicaux avec un nom similaire

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Device Recall ARTERIAL LINE KIT
  • Modèle / numéro de série
    Catalog Number: 194284, Lot Number: 99737820, Expiration Date: 2015-03.
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Distributed to United States (IL, AL, NY, TX, OK, MI, NC, CA, OH, VA, KY, CO, LA, WA, MO, AND IA) and Canada.
  • Description du dispositif
    ARTERIAL LINE KIT Arterial Line Kit #2 20ga X 3" REF/REORDER NO. 194284 Labeled Sterile, Rx. Argon Medical Devices, Inc. 1445 Flat Creek Road Athens, TX 75751 800-927-4669.
  • Manufacturer
    Argon Medical Devices, Inc
Device Recall ARTERIAL LINE KIT
  • Modèle / numéro de série
    Catalog Number: 498104, Lot Number: 99737777, Expiration Date: 2014-12.
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Distributed to United States (IL, AL, NY, TX, OK, MI, NC, CA, OH, VA, KY, CO, LA, WA, MO, AND IA) and Canada.
  • Description du dispositif
    ARTERIAL LINE KIT REF/REORDER NO. 498104 DISPOSABLE SINGLE USE, Rx. Argon Medical Devices, Inc. 1445 Flat Creek Road Athens, TX 75751.
  • Manufacturer
    Argon Medical Devices, Inc
Device Recall ARTERIAL LINE KIT
  • Modèle / numéro de série
    Catalog Number: 498410B, Lot Number: 99737665, Expiration Date: 2012-10.
  • Classification du dispositif
    Gastroenterology-Urology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed to United States (IL, AL, NY, TX, OK, MI, NC, CA, OH, VA, KY, CO, LA, WA, MO, AND IA) and Canada.
  • Description du dispositif
    ARTERIAL LINE KIT REF/REORDER NO. 498410B DISPOSABLE, SINGLE USE, Rx. Argon Medical Devices, Inc. 1445 Flat Creek Road Athens, TX 75751.
  • Manufacturer
    Argon Medical Devices, Inc
Device Recall ARTERIAL LINE KIT
  • Modèle / numéro de série
    Catalog Number: 498411B, Lot Number: 99736745, Expiration Date: 2012-10.
  • Classification du dispositif
    Gastroenterology-Urology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed to United States (IL, AL, NY, TX, OK, MI, NC, CA, OH, VA, KY, CO, LA, WA, MO, AND IA) and Canada.
  • Description du dispositif
    ARTERIAL LINE KIT REF/REORDER NO. 498411B DISPOSABLE SINGLE USE, Rx. Argon Medical Devices, Inc. 1445 Flat Creek Road Athens, TX 75751.
  • Manufacturer
    Argon Medical Devices, Inc
Device Recall ARTERIAL LINE KIT
  • Modèle / numéro de série
    Catalog Number: 498412B, Lot Number: 99716572, Expiration Date: 2011-12 and Lot Number: 99738188, Expiration Date: 2012-10.
  • Classification du dispositif
    Gastroenterology-Urology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed to United States (IL, AL, NY, TX, OK, MI, NC, CA, OH, VA, KY, CO, LA, WA, MO, AND IA) and Canada.
  • Description du dispositif
    ARTERIAL LINE KIT REF/REORDER NO. 498412B DISPOSABLE SINGLE USE, Rx. Argon Medical Devices, Inc. 1445 Flat Creek Road Athens, TX 75751.
  • Manufacturer
    Argon Medical Devices, Inc
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