BEUDAMED
    9 results · 49ms · 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 ×

    Sterling Healthcare Manufacturing

    FDA UDI
    The Rodon Group·00860005875511·Sterling Fluid Trap-Tip Swabs, Sterile, Flexibl...

    Sterling Healthcare Manufacturing

    FDA UDI
    The Rodon Group·00860005875504·Sterling Fluid Trap-Tip Swabs, Sterile, Standar...

    EXPEDIUM SI POLYAXIAL SCREW

    FDA Adverse Event
    Malfunction ·DEPUY RAYNHAM·Product code NKB·August 1, 2012

    MW5080358

    FDA Adverse Event
    Injury ·October 3, 2018

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·March 8, 2018

    PRECISETYPE BEADCHIP TEST HEA

    FDA Adverse Event
    Malfunction ·BIOARRAY SOLUTIONS LTD.·Product code PEP·November 12, 2014

    HEA 1.2 BEADCHIP KIT, SLIDE CE

    FDA Adverse Event
    Malfunction ·BIOARRAY SOLUTIONS LTD.·Product code PEP·July 9, 2015

    PRECISETYPE BEADCHIP TEST HEA

    FDA Adverse Event
    Malfunction ·BIOARRAY SOLUTIONS LTD.·Product code PEP·December 8, 2014

    PRECISETYPE HEA MOLECULAR BEADCHIP TEST

    FDA Adverse Event
    Malfunction ·BIOARRAY SOLUTIONS·Product code PEP·December 9, 2021