BEUDAMED
    32 results · 25ms · Sources: EU EUDAMED, US FDA

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    Z-LINK CERVICAL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NexxZr™ S / D-100-18-NS-WT00-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271153708·

    ZAVATION F3D-Z CIF

    FDA UDI
    Zavation LLC·00197157020996·F3D-Z CIF 16mmx18mmx5mm - 10deg

    ACIF Interbody System

    FDA UDI
    Tyber Medical, LLC·M695M2C141005S0·ACIF TYPEEK Coated 14mm x 10mm, 0 deg Straight

    ASTRA TECH IMPLANT SYSTEM, NEW COMPONENT

    FDA 510(k)
    FDA Class 2 ·Dental

    GAMBRO PRISMAFLEX AND GAMBRO PRISMAFLEX M60 & M100 SETS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    9616026-2006-00240

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616026-2006-00244

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    9616026-2006-00239

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    9616026-2006-00222

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    9616026-2006-00252

    FDA Adverse Event
    Other ·Product code FII·June 21, 2006

    9616026-2006-00245

    FDA Adverse Event
    Malfunction ·Product code FII·June 22, 2006

    9616026-2006-00253

    FDA Adverse Event
    Other ·Product code FII·June 21, 2006

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 29, 2024

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

    HAMILTON-T1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·November 14, 2023

    9616026-2006-00221

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006