BEUDAMED
    15 results · 20ms · Sources: EU EUDAMED, US FDA

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    Torqr Intracardiac Electrode Catheter, Soloist Intracardiac Electrode Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780181880·Integra® Jarit® Meyerding Finger Retractor, 7",...

    NA

    FDA UDI
    GENDRON, INC.·00842307100041·STRETCHER,BARIATRIC TRANSPORT WITH HYD. FOWLER

    CETRA

    FDA UDI
    Orthofix US LLC·18257200120352·1-LEVEL PLATE ASSEMBLY, 32MM

    Ophthalmic Retractor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668101094·HELVESTON "BIG BARBIE" RETRACTOR 9MM

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100132611·IN-OVATION® C Roncone 022 U3-3 CS HK

    IN-OVATION® C

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K100132101·IN-OVATION® C Base Rx 022 U3-3 CS HK

    NA

    FDA UDI
    GENDRON, INC.·00842307103073·STRETCHER,BARIATRIC WITH POWDER COAT ...

    MUSE CARDIOLOGY INFORMATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAXMORESPINE SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 19, 2013

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·June 11, 2013

    ATRICURE WOLF LUMITIP DISSECTOR

    FDA Adverse Event
    Injury ·ATRICURE, INC.·Product code FTD·January 17, 2007

    HEARTMATE II LVAS, EUROPE

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·September 18, 2014

    PEN II MYLAN 3.0ML

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code NSC·October 22, 2019