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

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    BONNER BRACE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Greenwald Surgical Company, Inc.

    FDA UDI
    GRACE MANUFACTURING, INC.·10801334012342·McCrea Female Sound, Curved. 3/4-inch nominal b...

    Halyard

    FDA UDI
    Avanos Medical, Inc.·10680651442960·HYH-MIC,GTUBE,ENFIT-FTUB,-,24FR,1

    AVANOS

    FDA UDI
    Avanos Medical, Inc.·00350770442969·* MIC* Gastrostomy Feeding Tube with ENFit® Con...

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310K0100240·Caddie, Fixed Cross Links, 5.5mm Assembly

    Kalitec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0100240·SNII Tap, 4.50mm

    Matira

    FDA UDI
    Kalitec Direct LLC·B07307K0100240·Assembly, Caddie, Screws, Hinged

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0100240·Caddie, Fixed Cross Links, 5.5mm, Assesmbly

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·AUTOBAC MTS PLUS TEST SYTEM

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172972090·

    O2/CO2 NASAL FILTERLINE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SALVATION Midfoot Nail

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·AUTOBAC MTS PLUS TEST SYTEM

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·AUTOBAC MTS PLUS TEST SYTEM

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·AUTOBAC MTS PLUS TEST SYTEM

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA Pre-Market Approval
    FDA Class 2 ·AUTOBAC MTS PLUS TEST SYTEM

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·April 25, 2014

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code FZP·November 12, 2007

    TOTAL ASR FEM IMP SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·June 1, 2015