BEUDAMED
    14 results · 21ms · Sources: EU EUDAMED, US FDA

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    CALCIMOL LC

    FDA 510(k)
    FDA Class 2 ·Dental

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981239961·Interbody, 9mm x 24mm x 18mm, 22 Deg

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981240370·Trial, 9mm x 24mm x 18mm, 22 Deg

    R-800-SF

    FDA 510(k)
    FDA Class 1 ·Radiology

    PRECISION SYSTEMS ANALETTE CHEMISTRY ANALYZER STANBIO LABORATORY REAGENTS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AGC DA2000 KN TIB BRG 71/75X14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·August 31, 2016

    BIOMET AGC V2 INTERLOK TIBIAL 22X 67MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HRY·June 16, 2017

    AGC V2 INTERLOK TIB 10X 71MM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code HRX·May 19, 2017

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 14, 2012

    MAXIMO II DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·December 14, 2010

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    AGC V2 INTERLOK TIB 8 X 75MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·April 12, 2017

    AGC V2 INTERLOK TIB 8 X 79MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 22, 2016

    AGC REVISION KNEE TIBIAL AUGMENTATION

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code JWH·June 28, 2017