BEUDAMED
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    WRP FOLEYCATH

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

    CARIS SITE MARKER

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

    ITEM #273 CONTACT LENS CASES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MOTO PARTIAL KNEE TIBIAL INSERT FIX S4 RM - 8MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·April 23, 2020

    MOTO PARTIAL KNEE 02.18.003RM ANATOMICAL FEMORAL COMPONENT CEMENTED S3 RM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·March 13, 2024

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 30, 2014

    CAPIOX SX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTN·January 4, 2013

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 20, 2010

    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