BEUDAMED
    773 results · 21ms · Sources: EU EUDAMED, US FDA

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    Adaptive Biotechnologies clonoSEQ Assay

    FDA 510(k)
    FDA Class 2 ·Pathology

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377046925·RELINE-O Trial, 5mm H Lamina W L-pop

    Paradigm

    FDA UDI
    Proprio, Inc.·00850042604021·Paradigm General Instrument Set

    JEWELERS FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896084421·JEWELERS FORCEPS ANGLED TIP

    BONN SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896083448·BONN SCISSORS CURVED BLADE POWER CUT GOLD

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193113197·HA PEEK EVOS Straight, ,9mmx8mmx 22mm , FLAT 0...

    Zavation

    FDA UDI
    Zavation LLC·00842166131576·Ti3Z CIF 12mmx14mmx9mm -0 deg

    MicroAire®

    FDA UDI
    Microaire Surgical Instruments LLC·00847399000880·SMALL SAGITTAL SAW BLADE, 10.2mm X 17.8mm X 0.5mm

    NA

    FDA UDI
    STERILMED, INC.·10888551001526·SAW BLADE SAGITTAL

    BRACE EZE

    FDA 510(k)
    FDA Class 1 ·Dental

    SPIRAL RADIUS RODDING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TANDEM T:SLIM INSULIN DELIVER SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE INC.·Product code LZG·October 21, 2014

    STAT2® IV GRAVITY FLOW CONTROLLER, 20 DROPS/ML

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code FPA·August 10, 2011

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·July 1, 2013

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021

    Clarius Ultrasound Scanner

    FDA UDI
    Clarius Mobile Health Corp·07540205000595·Clarius brand C3 Premium scanner

    Clarius Ultrasound Scanner

    FDA UDI
    Clarius Mobile Health Corp·07540205000199·ARTHREX Synergy Curvilinear Scanner

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021