BEUDAMED
    24 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ENDOSCOPIC CLIP APPLIERS WITH CLIP MAGAZINE

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

    CD42b-APC

    FDA UDI
    Miltenyi Biotec B.V. & Co. KG·04049934134289·REA185 recognizes human CD42b, a 145 kDa, singl...

    VYSIS UROVYSION BLADDER CANCER RECURRENCE KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    URANUS, COMFORTOUCH LASER SYSTEM

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

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710810310160·Dwyer Calcaneal Guide, 31mm x 16mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710810310150·Dwyer Calcaneal Guide, 31mm x 15mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710810310140·Dwyer Calcaneal Guide, 31mm x 14mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710810310130·Dwyer Calcaneal Guide, 31mm x 13mm

    RU NOVOSIBIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 16, 2013

    ATLANTIS® ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWQ·July 12, 2017

    ST JOSEPHS PHOENIX, AZ 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code DWF·July 31, 2009

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWQ·May 2, 2017

    RU NOVOSIBRIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·April 11, 2013

    RU NOVOSIBIRSK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DWF·October 16, 2013

    CP87170 DE MUENCHEN

    FDA Adverse Event
    Death ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. REG. # 8010379·Product code KWA·April 26, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·April 14, 2011

    SENSORMEDICS

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 207, INC.·Product code LSZ·July 18, 2008

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·March 17, 2016

    CP87641 GB SOUTHAMPTON

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DWE·March 22, 2010