BEUDAMED
    670 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 ×

    star RF Electrode, VIVA RF Electrode

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694026994·2.0mm X 12mm Cannulated Headless Screw

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837023287·200mm Threaded Rod

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613085001·Sideport Knife, Angled, Guarded, 1.2mm, 6 Per Box

    HORICO

    FDA UDI
    Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1720125·Rotary diamond instrument

    HORICO

    FDA UDI
    Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1720122·Rotary Diamond Instrument

    FG Dental Burs

    FDA UDI
    BIOLINE DENTAL IMPLANT SYSTEMS LTD·07290119311644·

    REFLEXION SPIRAL VARIABLE RADIUS CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIGITAL RADIOGRAPHY

    FDA 510(k)
    FDA Class 2 ·Radiology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694068406·Cannulated 2.0 x 12mm Headless Screw Sterile Qty 5

    SANTORINI™ Corpectomy Cage System

    FDA UDI
    VB Spine LLC·10888857243125·Clip Inserter, Inner Shaft

    MAM

    FDA UDI
    Mam USA Corporation·00845296071729·Mini Cooler (water filled teether - pink)

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·February 14, 2012

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 22, 2011

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·September 18, 2008

    FIRST PICC

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES, INC.·Product code FOZ·February 3, 2012

    FIRST PICC

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES, INC.·Product code FOZ·February 3, 2012

    INTRALASE IFS

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA, LLC·Product code HNO·April 17, 2012

    INTRALASE IFS

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA, LLC.·Product code HNO·April 17, 2012