BEUDAMED
    29 results · 31ms · Sources: EU EUDAMED, US FDA

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    DEPUY CMW 1 GENTAMICIN BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Premier REAMERS

    FDA UDI
    PREMIER DENTAL PRODUCTS COMPANY·D6919053002·REAMERS PKG 6 21MM 10

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00530021·

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809844351·FOR MEN 20-30 MM HG KNEE HIGH CLOSED TOE LARGE ...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690129950·Retaining Bolt, Congruent or Ultra Insert, Revi...

    NA

    FDA UDI
    ZIMMER TRABECULAR METAL TECHNOLOGY INC.·00889024311930·

    TRIAGE TOX DRUG SCREEN CALIBRATION VERIFICATION CONTROLS, CATALOG #94002

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    STERILIZATION PROCESS INDICATOR TAPES MODEL CI112 & CI123

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    BACT/ALERT® FA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    BACT/ALERT® SN CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 6, 2019

    BACT/ALERT® SA CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·August 8, 2019

    ADVIA CENTAUR CKMB AND TROPONIN ULTRA ASSAY

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JHX·July 29, 2010