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

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    PALOMAR VECTUS LASER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Unity Total Knee System

    FDA UDI
    CORIN LTD·05056139243943·UNITY KNEE™ PS-C INSERT - Size 6 x 22mm

    Bard® Urethral Catheter

    FDA UDI
    C. R. Bard, Inc.·00801741030000·Bard® Tiemann Model Urethral Catheter Coude Tip

    Consolidated Comm - Admin - 24 Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588206226·Consolidated Comm - Admin - 24 Poly White

    M-Flex®

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·00816734020012·Blue Silicone Tungsten Maloney Esophageal Dilat...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450207598·

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517071641·

    ARTHROCARE CONTROLLER (SYSTEM 2000 AND 8000); ARTHROCARE CABLE; FOOT CONTROL; POWER CORD; AND WANDS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BELIMED STEAM STERILIZER, MODEL MST-V 3-3-6

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UV FLASH TRANSFER SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 10, 2011

    ASR ACETABULAR IMPLANT 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013

    VIKING XL

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·July 28, 2014

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 5 / Adult Silicone King LAD¿ Patient Size: >70kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    MEDTRONIC MINIMED 670G

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code CGA·December 6, 2016

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·January 28, 2026

    BAKRI TAMPONADE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code OQY·March 27, 2018

    BAKRI TAMPONADE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code OQY·May 14, 2018

    BAKRI TAMPONADE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code OQY·December 4, 2018