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

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    TRINITY ACETABULAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ArgenZ ST 98x12 ML A4B

    FDA UDI
    ARGEN CORPORATION, THE·D818130128·Dental porcelain/ceramic restoration kit

    Gyrus ACMI

    FDA UDI
    Gyrus ACMI, LLC·00821925013254·FORCEPS PROTECTO-SLEEVE

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450266878·

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376610740·Universal Variable Lateral Cross Connector, 28m...

    CADWELL DISPOSABLE MONOPOLAR / BIPOLAR / CONCENTRIC / FLUSH TIP /BALL TIP PEDICLE SCREW STIMULATOR PROBE,

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    RESURFX 1565NM LASER MODULE

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

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    REAMER SHAFT, MOD, TRINKLE 8.0X284 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWE·February 13, 2012

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021

    STERRAD® CYCLESURE® 24 BIOLOGICAL INDICATOR

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code FRC·May 24, 2013

    UNKNOWN IMPLANTABLE CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·September 30, 2014

    RESOLUTION CLIP CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·June 16, 2011