BEUDAMED
    15 results · 24ms · 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 ×

    Common Type Insulin Pen Needle, Safety Type Insulin Pen Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122261·Kwire .062x6" (1.6x150mm) Threaded

    Vilex Power Accessory

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731122278·KWire .062x6" (1.6x150mm)

    FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR MODEL KD-930

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HHF1 ECHELON MULTI-PURPOSE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    STERIS

    FDA Adverse Event
    Malfunction ·VILEX·Product code HTY·April 6, 2005

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·October 10, 2014

    PLMA DVC V11.51 1 N

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 3, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 30, 2011

    OSS POROUS IM STEM 18.5 X 225

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KRO·May 21, 2020

    MOD ARTHRO 7 DEG LCK COLLAR

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HSB·January 13, 2020

    MOD ARTHRO NL 1CM DIASL CNCTR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HSB·August 6, 2019

    XP-CR Tibial Tray - Interlok 67mm Item # 195271

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019

    MOD ARTHRO NL 1CM DIASL CNCTR

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HSB·January 13, 2020

    TI LOW PROFILE SCREW 6.5X40MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·October 24, 2013