BEUDAMED
    103 results · 22ms · Sources: EU EUDAMED, US FDA

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    Transit-Pellets

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

    ANAESTHETIC FACE MASK WITH ADJUSTABLE AIR CUSHION, SIZE 2, PAEDIATRIC, 22F

    FDA UDI
    Intersurgical Incorporated·05030267123575·ANAESTHETIC FACE MASK WITH ADJUSTABLE AIR CUSHI...

    SANTORINI™ Corpectomy Cage System

    FDA UDI
    VB Spine LLC·10888857020948·Solid Cage

    EXACTECH

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code LXH·May 5, 2022

    Minuteman

    FDA UDI
    Spinal Simplicity, LLC·M9431002220000·Minuteman G6, 12mm

    Vozzle

    FDA UDI
    MECTRA LABS, INC.·00817984010334·Vozzle Vacu-Irrigator DS

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702779745·ELVAREX 2/KNEE HIGH/SLANT-CLOSED TOE-ELEPHANTIA...

    NA

    FDA UDI
    STRYKER CORPORATION·04546540371201·Cordless Driver Small Aseptic Battery Kit

    EXACTECH

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code LXH·April 5, 2022

    EXACTECH

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code LXH·April 5, 2022

    EXACTECH

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code LXH·February 28, 2022

    POURCHEZ RETRO TWIN LUMEN CHRONIC HEMODIALYSIS CATHETER WITH SEPARATED TIPS (WITH AND WITHOUT SIDE HOLES)

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

    HM SURGICAL DRAPES HM SURGICAL EQUIPMENT COVER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ENDOPATH 5MM CURVED SCISSORS WITH MONOPOLAR CAUTERY

    FDA Adverse Event
    Death ·ETHICON ENDO-SURGERY·Product code GEI·June 14, 2000

    ZYDERM 1 COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·MCGHAN MEDICAL CORPORATION·Product code LMH·August 1, 2000

    LIFEPAK 9P DEFIBRILLATOR/MONITOR/PACEMAKER

    FDA Adverse Event
    Malfunction ·MEDTRONIC PHYSIO-CONTROL CORP.·Product code LDD·May 16, 2000

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·September 20, 2000

    9500 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·March 17, 2000

    U.S.S.C. POLYSORB 1

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORP.·Product code GAN·March 24, 2000

    0600620-HICKMAN 12.0FR. RDL & PI

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (PUERTO RICO)·Product code DQO·June 27, 2000