BEUDAMED
    60 results · 23ms · Sources: EU EUDAMED, US FDA

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    AVS AS PEEK SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450313091·

    NA

    FDA UDI
    STRYKER CORPORATION·07613327096620·Elite Angled Attachment

    N/A

    FDA UDI
    STRYKER CORPORATION·07613327592047·Elite Q 17 cm angled attachment

    POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, YELLOW COLOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CARESIDE GGT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    GALAXY G3 XSFT 3.5MM X 7.5CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·November 2, 2022

    TRIATHLON PS X3 TIBIAL INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·May 20, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 26, 2014

    TRIMA ACCEL AUTO RBC AND PLS SET

    FDA Adverse Event
    Other ·CARIDIANBCT·Product code LKN·May 27, 2011

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    TRIATHLON P/A CR BEADED #5L

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·January 29, 2024

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code OKS·August 19, 2014

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 13, 2017

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 5, 2017

    KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 5 / Adult Silicone King LAD¿ Patient Size: >70kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012