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

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    Aequalis Ascend Flex Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AEQUALIS STEM FOR FRACTURE D.6.5 HA-COATED

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·January 5, 2026

    DIAMONDBACK 360 DBX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COMFYSLEEVE 1-75 AND LYMPHAPOD SLEEVES, FOR USE WITH LP OPTIMAL AND PLUS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    I-STAT TROPONIN (CTNI) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code MMI·September 24, 2019

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 21, 2014

    CLINITRON RITEHITE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code INX·June 13, 2013

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 4, 2011

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·January 8, 2020

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·January 3, 2020