BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    BLAZER DX-20 DIAGNOSTIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MEDCOMP ASH SPLIT

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

    24G X 0.75IN (0.7 X 19 MM) ANGIOCATH PLUS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·August 29, 2019

    ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code MTA·April 29, 2013

    TRAUMA TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·April 13, 2011

    OXIMAX N-595 PULSE OXIMAZ

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code DQA·July 25, 2008

    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