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 ×

    Synapse PACS

    FDA 510(k)
    FDA Class 2 ·Radiology

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486019945·MCK PF TEMPLATE (8 LEFT)

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694009478·Cannulated Depth Gauge -- 4

    Humeris Shoulder

    FDA UDI
    FX SOLUTIONS·03701037303238·HUMERIS STEM TA6V SIZE 08 CEMENTED

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197058704·Button-end Probe, with eye Ø2mm, ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197058698·Button-end Probe, with eye Ø2mm, ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197058742·Button-end Probe, with eye Ø2mm, ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197058728·Button-end Probe, with eye Ø2mm, ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197058735·Button-end Probe, with eye Ø2mm, ...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197058711·Button-end Probe, with eye Ø2mm, ...

    REAMER SHAFT, MOD, TRINKLE 8.0X284 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWE·February 13, 2012

    COBAS INTEGRA CHLORIDE ELCTRODE GEN.2

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AMEDICA DRUG TEST THC, COC, OPI, AMP, MET, PCP, BAR, BZO, MDMA, OXY, TCA

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    RADIAL JAW 4 BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·July 13, 2011

    PERFORATOR DRIVER W/HUDSON END

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBE·June 10, 2013

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    MICROVASCULAR PLUG

    FDA Adverse Event
    Injury ·REVERSE MEDICAL·Product code KRD·September 8, 2021

    MICROVASCULAR PLUG

    FDA Adverse Event
    Injury ·REVERSE MEDICAL·Product code KRD·September 8, 2021

    PRESSIO ICP AND ICT MONITORING KIT, PARENCHYMAL WITH BOLT

    FDA Adverse Event
    Death ·SOPHYSA·Product code GWM·November 18, 2024

    PRESSIO ICP AND ICT MONITORING KIT, PARENCHYMAL WITH BOLT

    FDA Adverse Event
    Malfunction ·SOPHYSA·Product code GWM·November 18, 2024