BEUDAMED
    18 results · 21ms · Sources: EU EUDAMED, US FDA

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    MODEL 654 ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    LOGIQ

    FDA UDI
    GE Ultrasound Korea Ltd.·00195278722966·LOGIQ E10s R4

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123052·K-WIRE - DOUBLE TROCAR 1.0mm DIA x 75mm

    Mediflex Modular III Basic Laparoscopic Instruments

    FDA UDI
    FLEXBAR MACHINE CORPORATION·00842102103971·Modular 3 Babcock Forceps Complete w/ Ratchet...

    LOGIQ

    FDA UDI
    GE Ultrasound Korea Ltd.·00198953042793·LOGIQ E10s R5 Console

    CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HA MALLORY/HEAD POROUS FEMORAL STEM & HA MALLORY/HEAD POROUS LATERALIZED FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    M-H HA/PC 11X160MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·December 16, 2015

    M-H SOLID SHELL HA/PC DIA54MM LN24

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·March 1, 2016

    MALLORY-HEAD SHORT FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code MEH·July 28, 2017

    MALLORY-HEAD ACETABULAR SHELL 54MM POUROUS + HAP COATED

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code MEH·August 11, 2016

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 21, 2014

    SCREW-IN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 17, 2013

    MLRY-HD XR LAT POR FMRL 8MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 24, 2020

    INTERGRATED APD SET

    FDA Adverse Event
    Malfunction ·VANTIVE US HEALTHCARE LLC·Product code FKX·April 4, 2025

    M-H HA/PC 12X165MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·December 16, 2015

    3821521DE

    Certificate
    MDD Annex II Section 4·Fibralign Corporation·DEKRA Certification B.V.·1 Basic UDI-DI