BEUDAMED
    7 results · 21ms · 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 FDA Adverse Event ×

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

    UNKNOWN PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CORK·Product code MEH·February 9, 2011

    GE OEC 9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·March 11, 2008

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·December 23, 1997

    LINER 10 DEGREE ELEVATED RIM 32 MM I.D. FOR USE WITH 56 MM O.D. SHELL

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·April 18, 2022

    FEMORAL STEM 12/14 NECK TAPER SIZE 13 138 MM STEM LENGTH CEMENTLESS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·April 18, 2022

    SHELL POROUS WITH CLUSTER HOLES 56 MM O.D.

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 18, 2022