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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    TRUECARE BIOMEDIX INTRAVASCULAR ADMINISTRATION SET, TRUECARE BIOMEDIX EXTENSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Drive

    FDA UDI
    Drive Devilbiss Healthcare·00822383102214·CommodesBariatric Product Description: Commode,...

    Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089448579·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450263785·

    Drive

    FDA UDI
    Drive Devilbiss Healthcare·00612479222137·CommodesBariatric Product Description: Commode,...

    NON-STERILE POWDER- FREE PEACH COLOR, NITRILE EXAMINATION GLOVES WITH LANO-E AND PEPPERMINT CITRUS SCENT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    4CH FLEX SPEEDER

    FDA 510(k)
    FDA Class 2 ·Radiology

    C-QUR TACSHIELD

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code FTL·December 31, 2014

    C-QUR TACSHIELD

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code FTL·December 31, 2014

    C-QUR TRACSHIELD

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code FTL·December 31, 2014

    UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·May 9, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·September 23, 2014

    IN TOUCH ZU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·May 18, 2011

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 35

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code HWC·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 40

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 45

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 35

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019