BEUDAMED
    15 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Critical Alert CommonPath Enterprise

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZIRCONIA SYRINGE NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COLORADO CATHETER STERILESURE - NEW NAME PERFIC CATH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TRILOGY FM ACET SHL 52 OD UNIV

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 18, 2026

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 5, 2024

    VSP SYSTEM

    FDA Adverse Event
    Injury ·3D SYSTEMS·Product code DZJ·December 18, 2020

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 18, 2026

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 18, 2026

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 18, 2026

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 18, 2026

    FEMORAL HEAD +3.5X28MM DIA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 18, 2026

    AVENIR MULLER STEM 6 STANDARD

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·April 9, 2026

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·October 13, 2008

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 27, 2013

    PLUM XL PLS MIC/MAC

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 22, 2011