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

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    HOSKINS-BARKAN GONIOTOMY LENS 10MM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Ultraverse® 018

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741165221·Ultraverse® 018 PTA Balloon Dilatation Catheter...

    SP55 SYRINGE PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EMDS GENTAMICIN CALIBRATOR ITEM NO. 67628/95

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 30, 2024

    PHYSIOMESH

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·June 16, 2014

    CONSULTA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·October 19, 2010

    UNKNOWN DEPUY LM ALL-POLY TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·December 17, 2012

    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 200 MM, Silicone, Sterile, Item 431197.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020