BEUDAMED
    42 results · 22ms · 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 ×

    APAS Independence with IC Chromogenic MRSA BD Analysis Module; APAS Independence with IC Chromogenic MRSA TFS/S Analysis Module

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Conventional Lead Apron .5mm Small 22 X 33

    FDA UDI
    Flow X Ray Corporation·00843696123178·Conventional Lead Apron .5mm Small, Electric Blue

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964084805·Endo Carry-On Procedure Kit

    QUANTUM, MODELS SR, HR, DL; VASCULIGHT, MODELS SR, HR, VS, VX, DL

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

    BARIREP

    FDA 510(k)
    FDA Unclassified ·Unknown

    2520274-2013-05317

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·September 4, 2013

    2520274-2013-05320

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·September 4, 2013

    2520274-2013-05360

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·September 4, 2013

    2520274-2013-05363

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 4, 2013

    2520274-2013-05349

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 4, 2013

    2520274-2013-05246

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 4, 2013

    2520274-2013-05347

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·September 4, 2013

    2520274-2013-05361

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·September 4, 2013

    2520274-2013-05370

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 4, 2013

    2520274-2013-05255

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·September 4, 2013

    ETHILON NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·May 7, 2019

    ETHILON NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·May 7, 2019

    2520274-2013-05260

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·September 4, 2013

    OSIGRAFT (OP-1 IMPLANT OSTEOGENIC PROTEIN 1)

    FDA Adverse Event
    Injury ·STRYKER BIOTECH·Product code MPY·December 9, 2009

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code HXX·August 11, 2011