BEUDAMED
    26 results · 23ms · Sources: EU EUDAMED, US FDA

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    GRENGLOO

    FDA 510(k)
    FDA Class 2 ·Dental

    REMEL

    FDA UDI
    REMEL, INC.·00848838008139·MH Broth (5ml) 20/PK

    10% PVP; 10% PVP IN EBSS SOLUTION

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PALCERAM 49

    FDA 510(k)
    FDA Class 2 ·Dental

    POWERLINK SYSTEM

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·Product code MIH·December 21, 2010

    OMEGA-21 VERTEBRAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code MNH·February 21, 2020

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·March 27, 2013

    ENDOTRACHEAL TUBE, SPIRAL-FLEX, CUFFED, 6.0MM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·March 15, 2011

    STERRAD NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 12, 2008

    ILIAC SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019

    PEDICLE SCREW, UNKNOWN TYPE OR SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·August 30, 2021

    UNKNOWN LUMBAR IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·April 11, 2022

    CLOSURE TOP UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    CLOSURE TOP UNSPECIFIED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·April 20, 2021

    CLOSURE TOP UNSPECIFIED

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code MNH·April 20, 2021

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025

    POLARIS SCREW, DIA. 6.5 X UNKNOWN LENGTH

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE, INC.·Product code NKB·May 28, 2025