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

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    INNOVACON HCG UKTRA TEST DEVICE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CONSULT HCG TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·March 4, 2025

    CONSULT HCG URINE CASSETTE 5001 25T

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·September 9, 2019

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040064730·MOLAR BAND LR 1ST 32 (2)

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B58210623610·FORCEPS, DRESSING, DENTAL

    TINA-QUANT COMPLEMENT C3C TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    SYNTHES (USA) LOCKING PROXIMAL PLATING (L-PTP) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    XIA LP POLYAXIAL SCREW 6.5 X 40MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·September 20, 2011

    XIA ROD DIA. 6 X 480

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·June 2, 2011

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·January 14, 2011

    XIA BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code KWQ·May 2, 2011

    XIA SCREW 6, 5 X 40

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code MNI·May 11, 2011

    XIA LP POLYAXIAL SCREW 5.5 X 45MM

    FDA Adverse Event
    Injury ·STRYKER SPINE-SWITZERLAND·Product code KWP·September 7, 2016

    XIA POLYAXIAL SCREW 8.5 X 40MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code MNH·May 2, 2011

    XIA BLOCKER

    FDA Adverse Event
    Injury ·STRYKER SPINE BORDEAUX·Product code KWP·May 11, 2011

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·January 19, 2011

    VOYAGER NC CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·December 4, 2008

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 16, 2013

    RUSCH ENDOTRACHEAL TUBE, SAFETY CLEAR, 7.5 MM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·March 18, 2011

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 18, 2008