BEUDAMED
    15 results · 25ms · Sources: EU EUDAMED, US FDA

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    STENTBOOST REL. 4

    FDA 510(k)
    FDA Class 2 ·Radiology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517637031·CoRoent Ant TLIF PEEK, 13x12x30mm 15°

    AGXO

    FDA UDI
    Oticon A/S·05707131258083·H150, MINIBTE 312 WL 85 SGR AGXO

    N/A

    FDA UDI
    TETRA MEDICAL SUPPLY CORP.·00614138210745·NEOPRENE SLIP-ON ELBOW SLEEVE, XXLARGE

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857560659·Trial With Stop Size 12x14x8 mm, 4 Degrees

    CLYDESDALE PTC SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·October 17, 2019

    OMRON INTELLISENSE DIGITAL BLOOD PRESSURE MONITOR, MODEL HEM-907XL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P

    FDA 510(k)
    FDA Class 2 ·Dental

    GENISTRONG

    FDA Adverse Event
    Malfunction ·GENICON·Product code GCJ·October 15, 2017

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code NKB·May 29, 2013

    LINOX SD 65/16

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO., KG·Product code LWS·June 13, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019

    Depuy SIGMA RP TC3 insert; polyethylene tibial insert, Sz 2.5, 30.0 mm; Ref 96-2338.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005