BEUDAMED
    75 results · 23ms · 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 ×

    Sorbact Wound Dressing-Ribbon Gauze

    FDA 510(k)
    FDA Unclassified ·Unknown

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776172817·RIGHT ANGLE MITER WITH LONG SERRACTIONS

    AOS HUMERAL NAIL 7.0mm x 22.5cm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665016840·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694032735·Oracle 25mm Cranial Distractor

    Symmetry Mixter

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482056813·Symmetry® Forceps, Mixter Right Angle, w/Serrat...

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111135057·MICRO MOSQUITO CRVD 5"

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122230·KWire .045x9" (1.1x225mm)

    PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 8.5 MM MODEL 03-1001, PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 10 MM MODEL 03-1

    FDA 510(k)
    FDA Class 2 ·Dental

    INNOVASA STAT*SEAL TOPICAL HEMOSTAT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OVUM ASPIRATION NEEDLE SINGLE LUMEN

    FDA Adverse Event
    Injury ·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 19, 2018

    OVUM ASPIRATION NEEDLE SINGLE LUMEN

    FDA Adverse Event
    Injury ·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 22, 2018

    OVUM ASPIRATION NEEDLE SINGLE LUMEN

    FDA Adverse Event
    Injury ·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 18, 2018

    OVUM ASPIRATION NEEDLE SINGLE LUMEN

    FDA Adverse Event
    Injury ·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 19, 2018

    OVUM ASPIRATION NEEDLE SINGLE LUMEN

    FDA Adverse Event
    Injury ·WILLIAM A. COOK AUSTRALIA, PTY LTD·Product code MQE·April 22, 2018

    STERRAD 200, SINGLE DOOR

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 14, 2013

    COULTER LH750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·July 1, 2011

    FREESTYLE FLASH

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 17, 2008

    HF UNIT "ESG-400"

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GEI·April 23, 2021

    HF UNIT "ESG-400"

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code GEI·December 5, 2017

    HF UNIT "ESG-400"

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GEI·July 8, 2020