BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    PENOX HOSPITAL BED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·August 5, 2020

    DIXON SCISSORS, STARINLESS STEEL, OPERATING TYPE

    FDA 510(k)

    7.5 MHZ LINEAR ARRAY SONOLINE PROBE

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·June 10, 2014

    SEPRAMESH IP

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·October 4, 2010

    SPECTRUM WIRELEES BATTERY MODULE B

    FDA Adverse Event
    Malfunction ·BASXTER HEALTHCARE CORP.·Product code FRN·November 9, 2012

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·May 5, 2020

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024