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

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    NP Cement HV Genta;NP Cement LV Genta;NP Cement HV System Genta;NP Cement LV System Genta

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Procure

    FDA UDI
    Keystone Industries·H66891431001·Hard Reline Professional Kit

    V. Mueller

    FDA UDI
    STERIS CORPORATION·10885403279249·V. Mueller DISPOSABLE BIPOLAR FORCEPS

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702435788·Elvarex Forte 3/Thigh High/Closed Toe-Elephanti...

    Perfect Fit

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377020551·Perfect Fit™Effort Belt Strap, XL, 60", 2 Pack

    Perfect Fit

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377020568·Perfect Fit™Effort Belt Strap, XXL, 75", 2 Pack

    Perfect Fit

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377020520·Perfect Fit™Effort Belt Strap, Medium, 30", 2 Pack

    Perfect Fit

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377020537·Perfect Fit™Effort Belt Strap, Large, 45"

    Perfect Fit

    FDA UDI
    DYMEDIX DIAGNOSTICS, INC.·00817377020544·Perfect Fit™Effort Belt Strap, Large 45", 2 pack

    BIO-MODULAR SHOULDER SYSTEM WITH HYDROXYAPATITE (HA) COATED GLENOID COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MOUNTAINEER OCT SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MetaSystems Probes

    FDA UDI
    MetaSystems Probes GmbH·04251315817494·XL PAX5 BA, Break Apart Probe

    SURESTEP ENHANCED

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·April 29, 2002

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 12, 2016

    M2A 38MM MOD HD -6MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 3, 2013

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 23, 2014

    OCTRODE 60-CM LENGTH PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 23, 2011

    POLY PER-Q-CATH SINGLE LUMEN PICC CATHETER, MODEL 3143100; POLY PER-Q-CATH DUAL LUMEN PICC CATHETER, MODEL 3246100

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ECHELON

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·February 19, 2025

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·January 15, 2008