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

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    KYPHON INFLATION SYRINGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CapSure® Spine System

    FDA UDI
    Spine Wave, Inc.·10840642129854·PS3 Tap, 4.5mm, NAV-M

    NA

    FDA UDI
    STRYKER CORPORATION·04546540216496·3.25:1 Keyed Chuck

    HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3

    FDA 510(k)
    FDA Class 2 ·Neurology

    AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ EPIDURAL NEEDLE, MODEL RM2035L

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 30, 2025

    AVEA VENTILATOR

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code CBK·July 17, 2015

    VALIANT CAPTIVIA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·May 9, 2013

    JOSTENT GRAFTMASTER

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MAF·September 19, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·May 25, 2011

    UNKNOWN FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 8, 2019

    UNKNOWN FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 8, 2019

    UNKNOWN FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 8, 2019

    UNKNOWN CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·February 6, 2019

    UNKNOWN CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 6, 2019

    UNKNOWN FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·February 8, 2019

    UNKNOWN FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 8, 2019

    UNKNOWN FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 8, 2019

    COCR HEAD SIZE 40MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·February 5, 2019

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·February 6, 2019