BEUDAMED
    25 results · 20ms · 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 ×

    BePOD Cannulated Arthrodesis Screws

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMR MAXI CABINET, ALUMINUM COMPOSITE, STANDARD, STORAGE-NO ELECTRICAL

    FDA UDI
    GLOBAL SURGICAL CORPORATION·00810040252556·

    Surgidac

    FDA UDI
    Covidien LP·20884521126999·Polyester Triple Stitch Reload

    Mariner Cortical

    FDA UDI
    Seaspine Orthopedics Corporation·10889981168674·CORTICAL SHANK, Cannulated, 7.0 X 40

    MSI

    FDA UDI
    Modern Surgical Instruments LLC·00810130203840·MF-Skull Clamp

    Mariner Cortical

    FDA UDI
    Seaspine Orthopedics Corporation·10889987168678·CORTICAL SHANK, Cannulated, 7.0 X 40

    Dukal

    FDA UDI
    Dukal LLC·20665973032591·Pretreat Gauze 4x4, 12ply, Green

    Ø3.5mm x 40mm Precontoured Cervical Rods

    FDA UDI
    XENCO MEDICAL LLC·B064XM21700401·

    BIOHARNESS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDERED VINYL PATIENT EXAMINATION GLOVES, WHITE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Ø3.5mm X 40mm PRECONTOURED CERVICAL RODS

    FDA UDI
    XENCO MEDICAL LLC·B064XMPH21700402·

    AQUILEX FLUID CONTROL SYSTEM

    FDA Adverse Event
    Malfunction ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIG·March 12, 2020

    TRULIANT TIB IMP CRC INSERT SZ 4, 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 30, 2022

    AMS AST For the In vitro quantitative determination of AST in serum Quantitative determination of AST in serum.

    FDA Recall
    Terminated ·AMS Diagnostics, LLC·Product code NJT·February 11, 2014

    LOCKSCR Ø2.4 SELF-TAP L16 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·June 14, 2013

    SYNCHROMED II

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code LKK·July 18, 2011

    ACCU-CHEK ® COMPACT PLUS TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 14, 2014

    AMS BUN UREA NITROGEN For the In vitro quantitative determination of Urea Nitrogen in serum Quantitative determination of Bun in serum.

    FDA Recall
    Terminated ·AMS Diagnostics, LLC·Product code NJT·February 11, 2014

    AMS URIC ACID For the In vitro quantitative determination of Uric Acid in serum Quantitative determination of Uric Acid in serum.

    FDA Recall
    Terminated ·AMS Diagnostics, LLC·Product code NJT·February 11, 2014

    TRULIANT TIB IMP PS INSERT SZ 3.5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 23, 2024