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

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    TUNNELING STYLET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEMETECH POLYDIOXANONE SYNTHETIC MONOFILAMENT (PDO) ABSORBABLE SUTURE

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

    React 71 Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·June 11, 2024

    FENESTRATED BIPOLAR FORCEPSINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 18, 2014

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·October 25, 2010

    COMFORTDRIVE 200XDR

    FDA Adverse Event
    Malfunction ·KAVO DENTAL GMBH·Product code EFB·December 17, 2012

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

    G7 HI-WALL E1 LINER 40MM H

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWZ·January 14, 2020

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·July 3, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·May 9, 2024

    DEMEDIOX

    FDA Adverse Event
    Injury ·DEMETECH CORPORATION·Product code NEW·February 23, 2024

    Hand Pack, part number AMS3640 Hand Pack, part number AMS4213(A Hand Pack, part number AMS4311(A Hand Pack, part number AMS5343 Hand Pack., part number PSS1843(A

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017