BEUDAMED
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    CERAMICS2IN1

    FDA 510(k)
    FDA Class 2 ·Dental

    Cattell T-Tube

    FDA UDI
    C. R. Bard, Inc.·00801741050428·Cattell T-Tube, X-Ray Opaque Rubber, 10 Fr

    COOLEY AORTIC CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921001500·COOLEY AORTIC CLAMP CURVED JAW CURVED SHANK

    ROCHESTER CARMALT FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896046252·ROCHESTER CARMALT FORCEPS STRAIGHT CROSS SERRAT...

    COOLEY AORTIC CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896002029·COOLEY AORTIC CLAMP CURVED JAW CURVED SHANK

    Astral 100/150

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Astral 100/150

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694033138·18mm Right L Rigid Plate & 18mm Left L Rigid Pl...

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555102100150·Straight Rod 6.0mm, 150mm

    KONAN CLINIC MICROSCOPE CLM-100-150

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 23, 2024

    VACUETTE TUBE 2 ML 9NC COAGULATION SODIUM CITRATE 3.2% 13X75

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE NA INC.·Product code GIM·March 30, 2021

    R & D SYSTEMS XERET HEMATOLOGY CONTROL

    FDA 510(k)
    FDA Class 2 ·Hematology

    64 CHANNEL EEG / MODEL NUMBER EX-NW-64

    FDA 510(k)
    FDA Class 2 ·Neurology

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 8, 2013

    I-STAT TROPONIN (CTNI) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code MMI·September 18, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·May 12, 2011

    MEDEX

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·June 17, 2021

    MEDEX

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·June 17, 2021

    PASSEO-14 2.5/100/150

    FDA Adverse Event
    Malfunction ·BIOTRONIK AG·Product code LIT·November 27, 2017