BEUDAMED
    25 results · 19ms · Sources: EU EUDAMED, US FDA

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    MS-30 FEMORAL STEM STANDARD AND LATERAL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PF-VIRTEC SYSTEM CMTED LAT.6

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LZO·August 6, 2019

    Humelock II Cemented Reversible Shoulder

    FDA UDI
    FX SOLUTIONS·03701037300121·HUMERAL CUP STANDARD PE/TA6V Ø40/+3

    FX V135 Shoulder Prosthesis

    FDA UDI
    FX SOLUTIONS·03701037315330·FX V135 HUMERAL CUP 135/145° STANDARD PE/TA6V Ø...

    Humelock II Cemented Reversible Shoulder

    FDA UDI
    FX SOLUTIONS·03701037303474·TRIAL HUMERAL CUP 135/145° Ø40+3

    POWDER-FREE LATEX EXAMINATION GLOVES-BLUE COLOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CEFAR MEDICAL AB CEFAR PRIMO

    FDA 510(k)
    FDA Class 2 ·Neurology

    H.A.M. Breast Applicator, 06-Channel

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020574·

    H.A.M. Breast Applicator, 08-Channel

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020598·

    H.A.M. Breast Applicator, 02-Channel

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020536·

    H.A.M. Breast Applicator, 10-Channel

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020611·

    H.A.M. Breast Applicator, 03-Channel

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020543·

    H.A.M. Breast Applicator, 09-Channel

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020604·

    H.A.M. Breast Applicator, 04-Channel

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020550·

    H.A.M. Breast Applicator, 05-Channel

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020567·

    H.A.M. Breast Applicator, 07-Channel

    FDA UDI
    MICK RADIO NUCLEAR INSTRUMENT, INC·00817330020581·

    LYNX

    FDA UDI
    HNM TOTAL RECON LLC·00841742112169·LYNX Distal Humeral Locking Plate Medial Anatom...

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·April 8, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·May 9, 2008

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 6, 2011