BEUDAMED
    33 results · 32ms · 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.
    Filters Regulation: Us FDA ×

    MONITOR B40

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIFESHIELD LATEX-FREE PRIMARY IV PUMP SET DISTAL MICROBORE PATIENT LINE, CONVERTIBLE PIN, 72 INCH, WITH 2 PRESSURE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MIM 5.2 (BRACHY)

    FDA 510(k)
    FDA Class 2 ·Radiology

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·May 28, 2014

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·March 21, 2014

    ACTIV.A.C.¿ THERAPY SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC.·Product code OMP·February 12, 2018

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·BBRAUN MEDICAL SAS·Product code LJT·July 1, 2015

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·April 11, 2014

    CELSITE

    FDA Adverse Event
    Injury ·B .BRAUN MEDICAL SAS·Product code LJT·February 20, 2017

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·September 14, 2015

    CELSITE

    FDA Adverse Event
    Injury ·B.BRAUN MEDICAL SAS·Product code LJT·April 8, 2020

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·March 21, 2014

    CELSITE

    FDA Adverse Event
    Injury ·B .BRAUN MEDICAL SAS·Product code LJT·August 3, 2017

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·July 10, 2014

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·May 29, 2013

    ACCU-CHEK MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·August 22, 2008

    EON MINI IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 16, 2011

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·July 6, 2015

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·December 9, 2014

    CELSITE ACCESS PORT

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL SAS·Product code LJT·February 27, 2014