BEUDAMED
    22 results · 29ms · 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 ×

    IODOSORB

    FDA 510(k)
    FDA Unclassified ·Unknown

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319742044·Spratt (Brun) Bone Curette 9" (22.5cm), straigh...

    AKITA JET

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MONACO RTP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code INK·June 26, 2013

    AFFINITY 4

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code HDD·October 6, 2008

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 26, 2011

    OSS-K DIAPHYSEAL SEGMENT 4CM W/SCREWS

    FDA Adverse Event
    Injury ·.·Product code JDI·May 5, 2017

    OSS POROUS COATED BOWED IM STEM W/SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS AXLE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS POROUS COATED BOWED IM STEM W/SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS FEMORAL BUSHINGS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS 16MM TIBIAL BEARING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS TIBIAL BUSHING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS-K 67 MM MODULAR POROUS COATED W/PLUG TIBIAL BASE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS POROUS COATED IM STEM W/SCREW - 11.5 MM X 90 MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS LOCKING PIN

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS SEGMENTAL FEMORAL - LEFT 7 CM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    OSS TM YOKE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 5, 2017

    Alinity i Ferritin Reagent Kit, List Number 07P6530 The Alinity i Ferritin assay is a chemiluminescent microparticle immunoassay (CMIA) used for the quantitative determination of ferritin in human serum and plasma on the Alinity i analyzer.

    FDA Enforcement
    Class II ·Terminated·Abbott Ireland Diagnostics Division·August 14, 2019