BEUDAMED
    51 results · 22ms · Sources: EU EUDAMED, US FDA

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    FLOCATH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950018116·FORCEP TISSUE 1X2 TEETH 4-1/2" 11.5CM

    Bio2 Technologies

    FDA UDI
    BIO2 TECHNOLOGIES, INC.·B01010000701·VITRIUM C SMALL, 5 x 20

    AP204-01- MICROBORE INFUSION SET WITH NON-VENTED SPIKE, FX ADMINISTRATION CASSET

    FDA UDI
    EITAN MEDICAL LTD·17290109153107·

    TAURUS

    FDA UDI
    CTL Medical Corporation·00841732150713·5.5mm Curved Rod 70mm Ti Alloy

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981172589·Axial, Closed, 70mm

    AP204 MICROBORE WITH NON-VENTED SPIKE, 0.2 FILTER AND BACK CHECK VALVE

    FDA UDI
    EITAN MEDICAL LTD·17290109159260·

    MD-Max ULIF

    FDA UDI
    PRECISION SPINE, INC.·00840019925976·Medial Retractor Blade, 70 mm

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2520000700·Curved Titanium Rod

    Taurus Pedicle Screw System

    FDA UDI
    SINTX Technologies, Inc.·M55525200075·Taurus Pedicle Screw System-Curved Rod 5.5x70mm

    Taurus Pedicle Screw System

    FDA UDI
    SINTX Technologies, Inc.·M555252000070·Taurus Pedicle Screw System-Curved Rod 5.5x70mm

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555102000070·Curved Rod 6.0mm, 70mm

    IMMULITE CARBAMAZEPINE, IMMULITE 2000 CARBAMAZEPINE, CATALOG # LKCB1, LKCB5 & L2KCB2, L2KCB6

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MODIFICATION TO ISOBAR SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMALL BATTERY DRIVE II

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HWE·May 26, 2015

    HUDSON AQUAPAK 340 SW W/040 ADAPTOR, FREN

    FDA Adverse Event
    Malfunction ·TELEFELX MEDICAL·Product code BTR·March 8, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·February 18, 2011

    FREESTYLE FLASH

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC, USA·Product code LFR·February 15, 2008

    SMALL BATTERY DRIVE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HWE·August 8, 2016

    SMR GLENOID BASEPLATE STANDARD

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·June 29, 2022