BEUDAMED
    25 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    HARDYDISK RIFAMPIN, 5MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    JEWEL CAST III

    FDA 510(k)
    FDA Class 2 ·Dental

    POLYPROPYLENE NONABSORBABLE SURGICAL SUTURES, USP

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 27, 2025

    86-003537 CUSTOM ANESTHESIA KIT

    FDA Adverse Event
    Malfunction ·DEROYAL·Product code LRP·February 25, 2000

    86-003537 CUSTOM ANESTHESIA KIT

    FDA Adverse Event
    Malfunction ·DEROYAL·Product code LRP·February 25, 2000

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 2, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 14, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

    CLEARGLIDE EVH LONGVIEW W/SCIS

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 23, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

    CLEARGLIDE EVH SMALL W/SCISSOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·October 16, 2009

    CLEARGLIDE EVH LONGVIEW W/SCIS

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 9, 2009

    SLIDING MECHANISM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTD·February 28, 2013

    TRAPEASE PERMANENT VENA CAVA FILTER 55CM

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code DTK·March 1, 2011

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·February 26, 2008

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 24, 2009

    CLEARGLIDE EVH SMALL W/SCISSOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code GEI·November 3, 2009