BEUDAMED
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    OTOMEDICS SOFT TYMPANOSTOMY TUBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Reprocessed Large Bone Oscillating Saw Blade, 19.5 x 80 x 0.80mm

    FDA UDI
    SURETEK MEDICAL·B39050711781·

    NA

    FDA UDI
    STERILMED, INC.·10888551020534·SAW BLADE OSCILLATING LARGE BONE

    ME-92

    FDA UDI
    Conmed Corporation·10845854002339·OSCILLATOR BLADE, ME-92 COATED, 19.5 X 80 X 0.8...

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825011987·Oscillating Saw Blade

    WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR

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

    CEDIA DAU 6-ACETYLMORPHINE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    COCR FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·February 23, 2018

    TWICE-AS-TOUGH CUFFS, WRIST PAIR, KEY LOCK CUFF AND STRAP

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code FMQ·April 8, 2013

    STERRAD 100NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·April 27, 2011

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEM INC.·Product code JAA·July 10, 2008

    CT EXPRES

    FDA Adverse Event
    Injury ·BRACCO INJENEERING S.A.·Product code IZQ·September 27, 2023

    BD TEXIUM¿ NEEDLE-FREE SYRINGE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FMF·November 29, 2022

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012