BEUDAMED
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    VINTAGE AL

    FDA 510(k)
    FDA Class 2 ·Dental

    Baltic Denture System BD Load

    FDA UDI
    Merz Dental GmbH·D7091032165·Baltic Denture System BDLoad ↓ Mm7 PLSEum2DFm A...

    LINEZOLID, 30UG, BBL SENSI-DISC

    FDA 510(k)
    FDA Class 2 ·Microbiology

    OLDELFT THORASCAN MODEL NUMBER 180T

    FDA 510(k)
    FDA Class 2 ·Radiology

    2520274-2013-11055

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code FSM·April 3, 2013

    UNICEL® DXC 800 PRO SYNCHRON® CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·March 29, 2011

    STARCLOSE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MGB·April 18, 2008

    UNKNOWN STEM EXTREMITIES IMPL

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·April 1, 2021

    AIMING ARM/ RADIOLUCENT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDS·November 11, 2025

    GLENOSPHERE 36 MM DIAMETER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 8, 2021

    BASE PLATE 15 MM POST LENGTH UNCEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·October 8, 2021

    TECNIS SIMPLICITY

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code HQL·March 14, 2024

    CUP EXTREMITIES IMPL

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code PHX·April 6, 2021

    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