BEUDAMED
    24 results · 26ms · Sources: EU EUDAMED, US FDA

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    VERIFY BIOLOGICAL INDICATOR CHALLENGE PACK FOR VAPORIZED VH202 STERILIZATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ANIMEC, MODELS AM-2S-4 AND AM-2S-5

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRACISION HARMONIC SCALPEL SYSTEM, MODELS GEN01, GEN02, GEN03, HP052, HP053, HSA07

    FDA 510(k)
    FDA Unclassified ·Unknown

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·June 15, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    WAVEWRITER ALPHA PRIME 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 24, 2023

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 16, 2006

    EQUINOXE

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

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code IOR·May 3, 2013

    ENTERRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LNQ·September 16, 2014

    TRIMA ACCEL RBC AND PLS SET

    FDA Adverse Event
    Other ·CARIDIANBCT·Product code LKN·May 5, 2011