BEUDAMED
    49 results · 24ms · Sources: EU EUDAMED, US FDA

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    INFINITY TRIDENT NMT POD

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Catalyst CSR Shoulder System

    FDA UDI
    CATALYST ORTHOSCIENCE INC.·00851388006197·Glenoid Trial, Left, Large

    Ocata Anterior Cervical System

    FDA UDI
    Kalitec Direct LLC·B07308K0120030·Removal Sleeve

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024368996·SWIVEL CLAMP BAR 48 INCHES 48 INCHES

    ENDOSKELETON® TA

    FDA UDI
    TITAN SPINE, LLC·00191375051336·7 Deg Lordotic, Implant Caddy, Base, X-Large

    ONE TOUCH II

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·April 29, 2003

    HDI 5000 ULTRASOUND SYSTEM WITH EXTENDED FIELD OF VIEW IMAGING

    FDA 510(k)
    FDA Class 2 ·Radiology

    DRG REACTION CHAMBER/SAFETY TIP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC. SOMERVILLE·Product code GAM·May 9, 2003

    COATED VICRYL (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC. SAN ANGELO·Product code GAM·May 9, 2003

    TRIUMPH-1 PORT

    FDA Adverse Event
    Malfunction ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·April 29, 2003

    ABC ALUMINA CERAMIC INSERT

    FDA Adverse Event
    Injury ·STRYKER HOWMEDICA OSTEONICS·Product code MRA·December 8, 2003

    ABC ALUMINA C-TAPER HEAD

    FDA Adverse Event
    Injury ·STRYKER HOWMEDICA OSTEONICS·Product code MRA·December 8, 2003

    SUBTALAR M.B.A.

    FDA Adverse Event
    Injury ·KINETIKOS MEDICAL, INC.·Product code ISH·February 4, 2004

    TENET T-MAX SHOULDER POSITIONER (BEACH CHAIR)

    FDA Adverse Event
    Other ·SMITH AND NEPHEW, INC., ENDOSCOPY DIVISION·Product code GBB·September 22, 2005

    J-VAC RESERVOIR

    FDA Adverse Event
    Malfunction ·AVAIL MEDICAL PRODUCTS·Product code GCY·July 18, 2003

    ALTO

    FDA Adverse Event
    Injury ·ELA MEDICAL·Product code MRM·April 10, 2007

    NCP BIPOLAR LEAD

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·April 4, 2003

    HOMECHOICE AUTOMATED PD SET W/CASSETTE 4-PRONG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code FKX·August 7, 2003

    SYNCHROMED EL

    FDA Adverse Event
    Other ·RICE CREEK MANUFACTURING·Product code LKK·May 24, 2006