BEUDAMED
    54 results · 30ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO PROMPT L-POP

    FDA 510(k)
    FDA Class 2 ·Dental

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489105640·PowerChem Neoprene Exam Gloves, Large

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099648·MAX 1ST MOLAR RT&LT 100 BANDS

    GRADIA®

    FDA UDI
    Gc America Inc.·14548161392853·GRADIA® CERVICAL TRANSLUCENT CT3

    GRADIA®

    FDA UDI
    Gc America Inc.·D0470014941·GRADIA® CERVICAL TRANSLUCENT CT3

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001494·artVeneer life lower anteriors, UIS, D3

    ActivHeal

    FDA UDI
    ADVANCED MEDICAL SOLUTIONS LIMITED·15032749001491·SILICONE FOAM BORDER 12.5x12.5CM

    SYNCHRON SYSTEMS ACETAMINOPHEN (ACTM) REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SAFE TOUCH NATURAL RUBBER POWDERED LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GDC POWER SUPPLY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - FREMONT·Product code HCG·July 20, 2010

    OPTETRAK

    FDA Adverse Event
    Other ·EXACTECH, INC.·Product code HSH·March 5, 2013

    AXSYM TROPONIN-I ADV

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code MMI·February 25, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·February 19, 2008

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·September 25, 2022

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·January 26, 2024

    CAPIOX FX HOLLOW FIBER OXYGENATOR WITH HARDSHELL RESERVOIR, ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·August 10, 2023

    CAPIOX FX25

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·July 18, 2023

    CAPIOX FX15 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·September 3, 2025

    VUELOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    VEULOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020