BEUDAMED
    31 results · 22ms · Sources: EU EUDAMED, US FDA

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    AUDIO TECHNOLOGIES S:R.1

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Essential Kit

    FDA UDI
    MEDIVATORS INC.·40677964011007·Essential Kit includes DEFENDO Olympus 5-piece ...

    ODYSSEY®

    FDA UDI
    Microport Orthopedics Inc.·M684K00112421·

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001142·artVeneer life upper anteriors, BIL, A4

    TruFlex

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730015167·NiTi Thermal Lower 16x22 10 archwires per pack

    TruFlex™

    FDA UDI
    Ortho Organizers, Inc.·00190707126919·TRUFLEX NiTi Thermal Lower 16x22 (10pk)

    COMFORT LATEX POWDERED PATIENT EXAMINATION GLOVES WITH PROTEIN LABEL CLAIM CONTAINS 200 MICROGRAMS OR LESS OF TOTAL WATE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    REVERSE SHOULDER SYSTEM HUMERAL REVERSE HC LINER 39/+0MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·January 12, 2021

    ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·June 16, 1997

    SET SCREW DRIVER

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code HXX·May 20, 2022

    MULTI-AXIAL SCREW INSERTER, UNIVERSAL (POLARIS 5.5)

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code HXX·May 20, 2022

    T20 DRIVER - FINAL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code HXX·May 20, 2022

    MULTI-AXIAL SCREW INSERTER, UNIVERSAL (POLARIS 5.5)

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code HXX·May 20, 2022

    GLUMA DESENSITIZER POWERGEL

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH·Product code LBH·March 6, 2013

    BRIGHTSPEED

    FDA Adverse Event
    Other ·GE HANGWEI MEDICAL SYSTEMS CO., LTD.·Product code JAK·February 18, 2011

    CONTOUR TEST STRIPS (50)

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·February 15, 2008

    ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 31, 1997

    ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·January 7, 1998

    ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 23, 1997