BEUDAMED
    15 results · 36ms · Sources: EU EUDAMED, US FDA

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    YEAST DIALYSATE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699533·GENUMEDI PSS BLUE, SIZE I

    Beyes

    FDA UDI
    Beyes Dental Canada Inc·00990010300422·FG CARBIDE 170L

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78503011·Sprint II Bracket Roth .022" max. 3 left w. hook

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78503010051·Sprint II Bracket Roth .022" max. 3 left w. hook

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78503011001·Sprint II Bracket Roth .022" max. 3 left w. hook

    Sprint®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR78503010101·Sprint II Bracket Roth .022" max. 3 left w. hook

    MRIDIUM 3850 MRI PUMP SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NavSuite3 Kit

    FDA 510(k)
    FDA Class 2 ·Neurology

    BD ANGIOCATH¿ IV CATHETER 22 G X 1"

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·September 13, 2017

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 15, 2014

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0 CM

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·September 21, 2012

    EXTERNAL NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·June 17, 2015

    BD ANGIOCATH¿ IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FOZ·August 8, 2017

    Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 781358. 2. Model Number (REF): 782107. 3. Model Number (REF): 782136. 510(k) Numbers: K213516, K223458, K230972, K232030, K251397, K251808

    FDA Enforcement
    Class II ·Ongoing·Philips North America·May 6, 2026