BEUDAMED
    23 results · 21ms · Sources: EU EUDAMED, US FDA

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    VITEK 2 STREPTOCOCCUS INDUCIBLE CLINDAMYCIN RESISTANCE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VITEK® 2 AST-ST01 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·October 24, 2017

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190900130·13mm SM Fixed 10° Lordotic, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190900100·10mm SM Fixed 10° Lordotic, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190900080·8mm SM Fixed 10° Lordotic, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190900120·12mm SM Fixed 10° Lordotic, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190900090·9mm SM Fixed 10° Lordotic, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190900140·14mm SM Fixed 10° Lordotic, HiJAK™ Cervical

    HiJAK™ Cervical

    FDA UDI
    ATLAS SPINE, INC.·M68111190900110·11mm SM Fixed 10° Lordotic, HiJAK™ Cervical

    ULTRA-THIN SDS BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EXACTECH EQUINOXE, PLATFORM FRACTURE STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·December 1, 2006

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQY·March 27, 2007

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code DQY·December 28, 2006

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQY·March 5, 2007

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 28, 2006

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code DQY·April 12, 2007

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 2, 2019

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 7, 2013

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 2, 2011