BEUDAMED
    13 results · 213ms · Sources: EU EUDAMED, US FDA

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    VX130 Ophthalmic Diagnostic Device

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NA

    FDA UDI
    medmix Deutschland GmbH·ETDG1620672·Sterile Irrigation Needles are used specificall...

    RR - UP Facilities - 75V

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588120676·RR - UP Facilities - 75V

    Avalign

    FDA UDI
    Avalign Technologies, Inc.·00190776021139·V-Silicone Retainers

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776116781·V-Silicone Retainers

    ENDOSKELETON TO

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TEXTURED POWER FREE BP2000 (BUTADIENE POLYMER) EXAM GLOVES, NATURAL COLOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    1.7MM CABLE WITH CRIMP 750MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code JDQ·March 6, 2017

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·October 10, 2014

    GYNECARE TVT RETROPUBIC SYSTEM

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

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·July 12, 2011

    BD¿ SPECIALTY SYRINGES AND ACCESSORIES (FLU+SYRINGE 0.25-1ML)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·November 9, 2017

    PEDICLE SCREW LATERAL CONNECTOR L150

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·December 13, 2023