BEUDAMED
    11 results · 29ms · Sources: EU EUDAMED, US FDA

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    A.M.P.C.O. SKIN SCRUB TRAY

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ORTHO SUMMIT SAMPLE HANDLER

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code JTC·July 1, 1998

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BIO-LOGIC CEEGRAPH NETLINK

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACUMATCH GXL 15DEG LINER 28MM SZ H

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code LZO·April 1, 2024

    PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, CEMENTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·July 18, 2024

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·May 9, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·October 19, 2012

    ADVANTA BED

    FDA Adverse Event
    Injury ·HILL-ROM, INC.·Product code FNL·August 10, 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

    Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633 Product Usage: Partial Shoulder Replacement.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019