BEUDAMED
    47 results · 25ms · Sources: EU EUDAMED, US FDA

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    Powder-free Nitrile Patient Examination Glove, Green Colored, Non-sterile, Low Dermatitis Potential, and Tested for Use with Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Vanguard Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304680562·

    Vanguard Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304647800·

    FREEDOM STIM 100 AND 200 ELECTRODE AND LEADWIRE EXTENSION

    FDA 510(k)
    FDA Class 2 ·Neurology

    PHYSIOLOGICAL MONITOR, PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    I-STAT EC8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CHL·March 20, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 14, 2025

    INSERTER TRITANIUM TL

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code LXH·October 28, 2022

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 28, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 18, 2014

    BIOMET CC I-BEAM TRAY 71MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 31, 2018

    VANGUARD CR ILOK FEM-RT 65

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    BIOMET CC I-BEAM TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

    BIOMET CC I-BEAM TRAY 71MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    VANGUARD COMPLETE KNEE SYSTEM - CRUICIATE RETAINING INTERLOK FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

    UNKNOWN BIOMET ARCOM 3 PEG PATELLA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    VANGUARD CR ILOK FEM-RT 62.5

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    UNKNOWN BIOMET ARCOM PATELLA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

    VANGUARD CR ILOK FEM-LT 65

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018