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

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    HARDY DISK, PENICILLIN, 10 UNITS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Halyard

    FDA UDI
    Avanos Medical, Inc.·10680651302486·SURGPN,-,CSTMKT,-,OQ,5

    PediFlex

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132133316·PEDIFLEX STERILIZATION CASE - IMPLANTS AND INST...

    BR Surgical, LLC

    FDA UDI
    BR Surgical, LLC·00857556008277·Cystoscope, autoclavable, Ø 4mm, 0º, 302mm

    BR Surgical, LLC

    FDA UDI
    BR Surgical, LLC·00857556008338·Hysteroscope, autoclavable, Ø 4mm, 0º, 302mm

    FINAL ASSY 2100-REMOTE 18-BR

    FDA UDI
    PARKS MEDICAL ELECTRONICS, INC.·00816787020120·

    MAGNA 5000 PHASED ARRAY CTL SPINE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    LEVEEN NEEDLE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ZYDERM 1 COLLAGEN IMPLANT (1.5ML)

    FDA Adverse Event
    Injury ·MCGHAN MEDICAL CORP. (FREMONT)·Product code LMH·January 18, 2001

    BONE SCREW Ø6,5 H.45MM

    FDA Adverse Event
    Malfunction ·LIMACORPORATE S.P.A.·Product code LPH·November 3, 2021

    CANNULA, 8MM, REGULAR, IS2000

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code NAY·September 4, 2007

    CANNULA, 8MM, REGULAR, IS2000

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code GCJ·September 4, 2007

    CANNULA, 8MM, REGULAR, IS2000

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code GCJ·September 4, 2007

    CANNULA, 8MM, REGULAR, IS2000

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code GCJ·September 4, 2007

    ENDOWRIST PROGRASP INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code NAY·September 4, 2007

    60-00302-01 PEDI 1/P 60/CA

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code MKJ·August 13, 2019

    ASR ACETABULAR IMPLANT 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 12, 2013

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 17, 2011

    2.3 MM DRILL BIT FOR BIORAPTOR

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIV.·Product code HTW·February 14, 2008

    ImpellaCP SmartAssistSetAPAC, Delo1895; Product Code: 1000302;

    FDA Recall
    Open, Classified ·Abiomed, Inc.·Product code OZD·August 5, 2024