BEUDAMED
    39 results · 22ms · Sources: EU EUDAMED, US FDA

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    TRIAGE BNP CALIBRATION VERIFICATION CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    8000231

    FDA UDI
    LASER PERIPHERALS, LLC·00816469021346·550u Laser Fiber PL

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950016686·CURETTE ANTRALPLASTY CLEPPER TATUM #2 6-1/2" 16...

    PowerPICC SOLO

    FDA UDI
    Bard Access Systems, Inc.·00801741043529·Catheter Placement Kit

    Bio2 Technologies

    FDA UDI
    BIO2 TECHNOLOGIES, INC.·B01010002311·VITRIUM C MEDIUM, 8 x 23

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167700002310·

    CURE IVIEW

    FDA UDI
    MEDITECH SPINE, LLC·B167900002310·

    8000231

    FDA Adverse Event
    Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·July 1, 2022

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code JTC·February 1, 2000

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1700002310·

    CURE IVIEW

    FDA UDI
    MEDITECH SPINE, LLC·B167S1900002310·

    AQUANET, MODEL EC 2000

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    QUICKSCREEN PRO MULTI DRUG SCREENING TEST, MODEL 9153 PAT04

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 21, 2012

    MODERATE PROFILE MAMMARY IMPLANT

    FDA Adverse Event
    MCGHAN MEDICAL CORP.·Product code FTR·December 28, 1993

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·October 24, 2014

    DIRECTA-SPAN TISSUE EXPANDER

    FDA Adverse Event
    MENTOR CORP.·Product code LCJ·December 28, 1993

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·March 12, 2013

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 17, 2011

    MEDFUSION 3500 SYRINGE INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD, INC.·Product code FRN·January 24, 2008