BEUDAMED
    3,519 results · 42ms · Sources: EU EUDAMED, US FDA

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    RETRACTOR MINI HOHMANN

    FDA UDI
    Biomet Orthopedics, LLC·00887868448713·

    RETRACTOR MINI HOHMANN

    FDA UDI
    Biomet Orthopedics, LLC·00887868072031·

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749038934·Titan. micro-ring-forceps, crysta.dust,2.0x1.0x...

    Leaseir MHR Xcell

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Leaseir Technologies SLU

    FDA UDI
    LEASEIR TECHNOLOGIES SOCIEDAD LIMITADA.·08437019546014·The Leaseir MHR Xcell is a surgical laser instr...

    Leaseir MHR Xcell (console) (MHR-100b); Handpiece: Dual (810-b and Blend-b); Handpiece: Quad (810-b and Blend-b)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Protean

    FDA UDI
    SKELETAL DYNAMICS L.L.C.·00841506138367·Instrument, Mini-Hohmann Retractor, Small

    Geminus

    FDA UDI
    SKELETAL DYNAMICS L.L.C.·00841506102467·

    ALINITY M HR HPV AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code MAQ·November 14, 2024

    ALINITY M HR HPV AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code MAQ·December 5, 2024

    ALINITY M HR HPV AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code MAQ·December 5, 2024

    ALINITY M SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code OOI·December 11, 2023

    FETAL MONITOR

    FDA Adverse Event
    Death ·PHILIPS MEDIZINSYSTEME BOBLINGEN·Product code HGM·March 20, 2006

    FETAL MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code HGM·October 16, 2007

    AVALON FM30 FETAL MONITOR

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code HGM·December 1, 2017

    ARCOM XL HI-WALL LINER RINGLOC-X SZ 64 (RINGLOC SIZE 27)

    FDA Adverse Event
    Injury ·.·Product code LPH·January 13, 2017

    ALINITY M HR HPV AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code MAQ·January 9, 2024

    ALINITY M HR HPV AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code MAQ·February 14, 2024

    ALINITY M SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code OOI·December 20, 2023

    ALINITY M SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code OOI·January 9, 2024