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

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    COMPONENTS FOR CARDIOVASCULAR PROCEDURE KIT - HEAT EXCHANGER COILS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092130919·NobelActive™/Conical-compatible RP Straight Mul...

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964008984·Endo Carry-On Procedure Kit

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092116753·NobelActive™/Conical-compatible RP Straight Mul...

    PowerMidline

    FDA UDI
    Bard Access Systems, Inc.·00801741202209·Catheter Placement Kit

    RENEGADE HI-FLO MICROCATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STERIS AMSCO MILLENNIUM STEAM STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·March 3, 2023

    CS100 INTRA-AORTIC BALLOON PUMP, ENGLISH, 220V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·June 5, 2023

    CS100

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·July 23, 2014

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·January 30, 2024

    SYS98XT

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·July 23, 2014

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·June 14, 2023

    CS300

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·January 30, 2014

    CS300

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·July 23, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 27, 2013

    100CC SILICONE BULB EVACUATOR

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code GBX·February 18, 2011

    SAGB QUICKCLOSE WITH VELOCITY INJECTION PORT

    FDA Adverse Event
    Injury ·OBTECH MEDICAL SARL·Product code LTI·February 19, 2008

    COUPLER AC ZOOM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SàRL·Product code FEM·August 12, 2020

    ZUMA Z2 7F GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC·Product code DQY·June 12, 2020