BEUDAMED
    52 results · 28ms · Sources: EU EUDAMED, US FDA

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    I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOCK, HOMEPUMP, EASYPUMP)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    T3

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746045660·DB BRACKET SL T3 MAX LEFT CENTRAL 018 TQ=+17 A=+5

    Waterpik Opotow Temporary Cement

    FDA UDI
    WATER PIK, INC.·D686521173·Zinc oxide eugenol temporary dental cement

    MAJESTIK (TM) SHIELDED ANGIOGRAPHY NEEDLE, MODEL STAN18T71W-25, MAJESTIK (TM) SHIELDED ANGIOGTAPHY NEEDLE, SRAN18T71WR-5

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VALIDATE CHEM 1 CALIBRATION VERIFICATION TEST SET, MODEL 10001

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 16, 2016

    SLEEPEASY

    FDA Adverse Event
    Injury ·RESPIRONICS INC.·Product code BZD·April 12, 2012

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 6, 2010

    REMSTAR M SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·November 25, 2009

    M-SERIES DC POWER SUPPLY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·May 25, 2012

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPAEDIC INC.·Product code KWP·June 25, 2009

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWQ·July 23, 2009

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·August 30, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 16, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 23, 2011

    CD HORIZON ADANTA

    FDA Adverse Event
    Other ·MEDTRONIC SOFAMOR DANEK·Product code KWP·April 3, 2009

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPER·Product code KWP·June 10, 2009

    ARTICULEZE M HEAD 36MM -2

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code JDI·April 11, 2013

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·September 2, 2014

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·April 12, 2011