BEUDAMED
    75 results · 22ms · Sources: EU EUDAMED, US FDA

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    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·BBL SCEPTOR SYSTEM MICRODILUTION ANTIMICROBIC SUSC

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·BBL SCEPTOR SYSTEM MICRODILUTION ANTIMICROBIC SUSC

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·BBL SCEPTOR SYSTEM MICRODILUTION ANTIMICROBIC SUSC

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·BBL SCEPTOR SYSTEM MICRODILUTION ANTIMICROBIC SUSC

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·BBL SCEPTOR SYSTEM MICRODILUTION ANTIMICROBIC SUSC

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·BBL SCEPTOR SYSTEM MICRODILUTION ANTIMICROBIC SUSC

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·BBL SCEPTOR SYSTEM MICRODILUTION ANTIMICROBIC SUSC

    Sphero Attachment

    FDA UDI
    Preat Corporation·00842092113806·Sphero Block Abutment Nobel Active 3.0 x 3mm (1...

    BaseVac

    FDA UDI
    R. E. Morrison Equipment Inc·D13028000300·12 User Triple Pump Package | 230V 2Hp (x3) w/ ...

    HEARTLINE RYDER NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896006829·HEARTLINE RYDER NEEDLE HOLDER WITH LOCK TUNGSTE...

    SURETRACE

    FDA UDI
    Conmed Corporation·10653405004417·Adult Foam ECG Suretrace Conductive Adhesive Gel

    HEARTLINE RYDER NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09928000300·HEARTLINE RYDER NEEDLE HOLDER WITH LOCK TUNGSTE...

    Rampart O

    FDA UDI
    SPINEOLOGY INC.·M7402800030·16x35mm Trial

    IMPLANTABLE BIPOLAR CARDIAC PULSE GEN.

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SURETRACE ADULT ECG ELECTRODE

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code DRX·October 24, 2013

    SURETRACE ADULT ECG ELECTRODE

    FDA Adverse Event
    CONMED CORPORATION·Product code DRX·October 25, 2013

    SURETRACE ADULT ECG ELECTRODE

    FDA Adverse Event
    CONMED CORPORATION·Product code DRX·October 25, 2013

    SURETRACE ADULT ECG ELECTRODE

    FDA Adverse Event
    CONMED CORPORATION·Product code DRX·October 25, 2013

    SURETRACE ADULT ECG ELECTRODE

    FDA Adverse Event
    CONMED CORPORATION·Product code DRX·October 25, 2013

    SURETRACE ADULT ECG ELECTRODE

    FDA Adverse Event
    CONMED CORPORATION·Product code DRX·October 25, 2013