BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    0.014 FLOPPY & 0.014 INTERMEDIATE GUIDE WIRES W/PHOSPHORYLCHOLINE POLYMER COATING & 4CM RADIOPAQUE TIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERTE-STACK® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074018706·SPACER 2961232 CAPS VS PK VBS END 32X12

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295236092·P.F.C. SIGMA POSTERIOR-LIPPED TIBIAL INSERT TRI...

    ON-Q* EchoSpark Echogenic Catheter; ON-Q* T-bloc* Echogenic Continuous Nerve Block Kit

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006

    FDA 510(k)
    FDA Unclassified ·Unknown

    VERTE-STACK SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code MQP·April 18, 2013

    EMERALD

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL OPTICS·Product code KYB·July 6, 2016

    HEARTSTART XL+ DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 28, 2014

    EASYPUMP II LT 270-27-S

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL PRODUCTION LTD.·Product code MEB·February 8, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·January 11, 2011

    Mitek Screw and Washer Depth Gauge, Product Code 219024

    FDA Enforcement
    Class II ·Terminated·DePuy Mitek, Inc., a Johnson & Johnson Co.·October 31, 2018