BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    Q-Switched Nd: YAG Laser System

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

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197508230·Ferreira Style Breast Retractor 190x36...

    SINGLE-CHANNEL HANDHELD ELECTROCARDIOGRAPH, MODEL ECG80A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GYNECARE TVT ABBREVO CONTINENCE SYSTEM

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

    GYNECARE TVT-ABBREVO MINI LCM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·November 30, 2021

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·October 9, 2008

    6000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 14, 2013

    PO2 MICROPROBE 200 MM WITH SMART CARD

    FDA Adverse Event
    Malfunction ·GMS-GESELLSCHAFT FUR MEDIZINISCHE·Product code GWM·July 19, 2011

    Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020

    FDA Enforcement
    Class II ·Terminated·Cardinal Health 200, LLC·February 26, 2020