BEUDAMED
    14 results · 25ms · 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.

    OSCILLATING BONE SAW BLADE, 6200 SERIES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    IMMUNO-CRP

    FDA 510(k)
    FDA Class 2 ·Immunology

    ANTI-HUMAN LEU-2A (CD8) PE

    FDA 510(k)
    FDA Class 2 ·Hematology

    ELEVATE PROLAPSE REPAIR SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTP·January 28, 2013

    EON MINI IPG

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION DIV.·Product code LGW·November 23, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 1, 2014

    LOCKSCR 5 SELF-TAP L16 SST

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·July 8, 2021

    "2.7MM" SYSTEM EMERGENCY CROSS DRIVE SCREW, 1/PKG

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·October 25, 2018

    TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code LZD·October 25, 2018

    "2.4 MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 2.7 X 10 MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·October 25, 2018

    TMJ SYSTEM CROSS DRIVE FOSSA SCREW, 2.0 X 9 MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·October 25, 2018

    "2.4MM" SYSTEM HIGH TORQUE (HT)CROSS-DRIVE SCREW, 2.7X8MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·October 25, 2018

    TMJ SYSTEM CROSS-DRIVE FOSSA SCREW, 2.0 X 7 MM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·October 25, 2018

    "2.7MM" SYSTEM EMERGENCY CROSS DRIVE SCREW, 1/PKG

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·October 25, 2018