BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    Cannulated PediGuard Needle#1, Cannulated PediGuard Needle#2, Cannulated PediGuard Needle 120mm, Cannulated PediGuard Handle; PediGuard Tri Tip Ø4.0mm, PediGuard Tri Tip Ø3.2mm, PediGuard Tri Tip Ø2.5mm, PediGuard Ø2.5mm XS, PediGuard Curv, PediGuard Curv XS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·July 22, 2002

    CARDIO MED MODEL A102, H104, O101, P103, AND Z100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDER FREE CLEAR SYNTHETIC VINYL EXAMINATION GLOVES, SMALL, MEDIUM, LARGE, X-LARGE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973936·UniTip High Resolution Catheter 14F

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970959·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970935·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970942·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970911·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973028·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973806·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973240·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970966·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970928·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970973·

    PELVICOL ACELLULAR COLLIGEN MATRIX

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE·Product code FTL·May 24, 2013

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL ¿ NEUROMODULATION·Product code GZB·September 23, 2014

    RADIAL JAW¿ 3

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code KGE·June 28, 2011

    Cardio Medical Products, Inc. Defibrillation/Cardioversion/Monophasic or Biphasic Pacing/ECG Electrode Rx Only Single Patient Use Only Manufactured for Cardio Medical Products 385 Franklin Avenue, Suite L Rockaway, New Jersey 07866 www.cardiomedicalproducts.com (800) 227-3633 (973) 586-9624 FAX Defibrillator

    FDA Enforcement
    Class II ·Terminated·Cardio Medical Products·July 17, 2013

    1.8MM DRILL BIT WITH DEPTH MARK/QC/110MM

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HTW·December 18, 2019