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

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    Bausch + Lomb (Kalifilcon A) Soft Contact Lens, Bausch + Lomb (Kalifilcon A) Soft Contact Lens for astigmatism

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NA

    FDA UDI
    Synthes GmbH·10886982141286·1.0MM CORTEX SCREW SELF-TAPPING 8MM

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694006866·Holding Cap, 2.0mm Plates, Blunt Cannula

    BAILEY HEMOSTATIC FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896084865·BAILEY HEMOSTATIC FORCEPS ACUTE ANGLED EXTRA FI...

    INTRASTENT LD (LARGE DIAMETER) STENT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ACCUCLOT DRVVT CONFIRM, CATALOG NO. A62119

    FDA 510(k)
    FDA Class 1 ·Hematology

    EDWARDS ESHEATH+ INTRODUCER SET

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DYB·April 28, 2022

    UNKNOWN EDWARDS TRANSFEMORAL SHEATH

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYB·March 12, 2026

    TF SHEATH UNKNOWN

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DYB·July 18, 2023

    UNKNOWN EDWARDS LIFESCIENCES SHEATH

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYB·May 12, 2025

    EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES LLC·Product code NPT·December 5, 2024

    AKREOS ADAPT ADVANCED OPTICS ASPHERIC LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code HQL·October 19, 2012

    GEM VR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·October 6, 2017

    KAPPA 400 DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·October 11, 2018

    KAPPA 400 DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·October 11, 2018

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 11, 2011

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    UNKNOWN·Product code IKX·July 1, 2013

    Merge PACS

    FDA Enforcement
    Class II ·Terminated·Merge Healthcare, Inc.·September 16, 2020

    ESHEATH INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYB·December 17, 2021