BEUDAMED
    721 results · 13ms · Sources: EU EUDAMED, US FDA

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    ASY, Brat 2 Procedure Set

    FDA Recall
    Terminated ·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005

    ASY, Brat 2 Pack Procedure Set

    FDA Recall
    Terminated ·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005

    ASY Brat 2 Procedure Set

    FDA Recall
    Terminated ·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005

    ASY, Brat Pack Procedure Set

    FDA Recall
    Terminated ·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005

    ASY Brat 2 Procedure Set

    FDA Recall
    Terminated ·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005

    4Fr x 20cm Single Lumen CT Midline Basic Tray, Product Code: VYML4S1001

    FDA Recall
    Terminated ·Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.·Product code PND·September 24, 2019

    ASY Brat 2 Procedure Set, for blood recovery & autotransfusion.

    FDA Recall
    Terminated ·Cobe Cardiovascular, Inc·Product code CAC·June 22, 2005

    NIPRO SafeTouch II Safety AVF Needle, 17G x 1 inch. Item code FS+173230BC.

    FDA Recall
    Terminated ·Nipro Medical Corporation·Product code FOZ·April 1, 2014

    Product is labeled as LTX XP Miniplant, Dental Implant, Sterile.

    FDA Recall
    Terminated ·Product code DZE·August 3, 2007

    Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: The Applied Voyant Open Fusion Device is designed for use with the Voyant Electrosurgical Generator. The device is an advanced bipolar instrument that uses RF energy, provided by the generator, to seal vessels up to and including 5mm (EB040+) or 7mm (EB040) in diameter. The device may also be used to seal tissue bundles that can be captured in the device jaws. The system delivers the energy required to fuse the tissue between the jaws of the device by monitoring voltage and current throughout the seal cycle. The device also features a useractuated blade for the transection of sealed tissue.

    FDA Recall
    Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code GEI·July 31, 2015

    Myoglobin Test Card (Serum); LumiQuick,. Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014

    Tramadol Strip; LumiQuick. Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014

    Morphine Test Card (2000); LumiQuick, Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014

    Alcohol Test, Saliva; LumiQuick. Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014

    Rotavirus Test Card LumiQuick, Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014

    Methadone Test Strip; LumiQuick,. Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014

    Amphetamine Test Card; LumiQuick. Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014

    Cocaine Test Card; LumiQuick. Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014

    Methadone Test Card; LumiQuick. Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014

    Malaria pan Antigen Test; LumiQuick, Santa Clara, CA 95054

    FDA Recall
    Terminated ·LumiQuick Diagnostics Inc.·March 4, 2014