BEUDAMED
    88 results · 20ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO FLEXVIEW CLINICAL MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040008034·Zirlux 16+ C1 89x17x12

    Vac Attak™

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·00348783003895·VAC ATTAK SAMPLE (1pk)

    MetaSystems Probes

    FDA UDI
    MetaSystems Probes GmbH·04251315808072·XL EWSR1 BA, 10x 100µl, Break Apart Probe

    PROVIEW EYE PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GLOBAL FX POROUS-COATED HUMERAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·July 9, 1999

    SURGICAL STAINLESS STEEL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAQ·January 8, 2010

    CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Other ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·March 2, 1999

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·THE KENDALL CO.·Product code MGB·March 4, 1999

    CD HORIZON CONICAL CORE SCREW

    FDA Adverse Event
    Injury ·SOFAMOR DANEK EUROPE·Product code HWC·May 11, 1999

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·THE KENDALL CO.·Product code MGB·March 4, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·December 3, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·April 19, 2000

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·April 27, 1999

    ASSURANCE 2000 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·July 28, 1999

    UNKNOWN VESICA PERC STABILIZATIION KIT W/PROTEGEN

    FDA Adverse Event
    Injury ·MICROVASIVE UROLOGY/ A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code FTL·June 16, 2000

    CADENCE V-110C

    FDA Adverse Event
    Injury ·VENTRITEX·Product code LWS·July 9, 1999

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·December 1, 2006