BEUDAMED
    19 results · 24ms · Sources: EU EUDAMED, US FDA

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    FACIAL PREBENT PLATING WITH VIRTUAL SURGICAL PLANNING

    FDA 510(k)
    FDA Class 2 ·Dental

    RC Screw-retained Abutment

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600381242·

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668103258·JAFFE LENS SPATULA 0.5MM

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702930436·ELVAREX FORTE 3/KNEE HIGH/SLANT-OPEN TOE-ELEPHA...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702555080·E3/AD/SL-CT/NOP-I/CB

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702471854·ELVAREX 3/THIGH HIGH/CLOSED TOE/DOTTED 2,5 CM S...

    BECKER DOUBLE GRATER

    FDA UDI
    The Wells Johnson Company·B458201326000·Cannula, Becker Double Grater, specify length, ...

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·August 24, 2015

    VAXCEL PORT, MODEL 45-333 AND VAXCEL W/PASV PORT, MODEL 45-233

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SIMPLYGO BREAST PUMP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971383·

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    LIFEPAK® 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019

    AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - ANTERIOR

    FDA Adverse Event
    Injury ·BARD SHANNON LIMITED·Product code FTL·May 16, 2013

    INVACARE

    FDA Adverse Event
    Injury ·INVACARE·Product code FNG·June 13, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·August 22, 2008

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·October 24, 2019

    INTELLIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 24, 2018

    Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633 Product Usage: Partial Shoulder Replacement.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019