BEUDAMED
    8 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 ×

    SENTRY(TM) ANTERIOR/POSTERIOR SPINAL SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BBL CRYSTAL MRSA ID SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PATPOS GREEN

    FDA 510(k)
    FDA Class 1 ·Radiology

    PERF CON TIB BRG XSML 22X60

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code JWH·March 23, 2018

    HI-TORQUE WHISPER LS GUIDE WIRE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code DQX·January 30, 2013

    REPLY

    FDA Adverse Event
    Injury ·SORIN BIOMEDICA C.R.M., S.R.L.·Product code NVZ·December 15, 2010

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 15, 2014

    StemPro¿ MSC SFM CTS"

    FDA Enforcement
    Class II ·Terminated·Life Technologies Corporation·November 13, 2019