BEUDAMED
    23 results · 30ms · Sources: EU EUDAMED, US FDA

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    UNO

    FDA 510(k)
    FDA Class 2 ·Dental

    Key Surgical K-Wires and Steinmann Pins

    FDA UDI
    KEY SURGICAL, INC.·00849771012450·K-Wires, Single trocar, .035-inch (.9mm) diamet...

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292688·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049033·K-Wires, Single trocar, .035-inch (.9mm) diamet...

    K-Wire w. trocar/round end 0.89mm/102mm, 6 pcs./unit

    FDA UDI
    mahe medical gmbh·EMAHKM711310·K-Wire w. trocar/round end 0.89mm...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659484221·K-Wire w. trocar/round end _x000D_...

    Bone Screws

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132134436·7.0 CASE LID

    3D HDRAULIC FINE MICROMANIPULATOR MO-188NE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    METHADONE MICROPLATE EIA URINE APPLICATION

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ENDOPATH ETS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·November 7, 1997

    CLIK X MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 15, 2021

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    ANIMAS CORPORATION·Product code LZG·April 22, 2013

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code MCX·April 27, 2011

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 10, 2008

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·February 6, 1998

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 15, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 11, 2017

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code LCP·January 5, 2016