BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    IMPIX 3D Print Cages

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CLEARFIL MAJESTY POSTERIOR

    FDA 510(k)
    FDA Class 2 ·Dental

    ACCLARENT TYMPANOSTOMY TUBE AND TYMPANOSTOMY TUBE DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CANCELLOUS BONE SCREW FLAT HEAD Ø 6,5 L 45

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LZO·May 10, 2017

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code PAH·June 11, 2013

    VENTILATOR, CONTINUOUS, FACILITY USE

    FDA Adverse Event
    Other ·RESPIRONICS, INC.·Product code CBK·June 6, 2011

    RESTORE RECHARGEABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 17, 2008

    CANCELLOUS BONE SCREW FLAT HEAD Ø 6,5 L 35

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LZO·June 16, 2017

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·December 10, 2024

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·January 5, 2023