BEUDAMED
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    GLUCOSE (HEXOKINASE) LIQUID REAGENT, MODEL G518-150

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964001121·The ENDO CARRY-ON Procedure Kit contains all of...

    TruFlex

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730011749·NiTi U/L .014 10 archwires per pack

    TruFlex™

    FDA UDI
    Ortho Organizers, Inc.·00190707125127·TRUFLEX NiTi U/L .014 (10pk)

    eWave 6-Lead EKG

    FDA UDI
    Wearlinq, Inc.·K00010·Continuous wearable electrocardiogram (ECG) mon...

    EnPlace

    FDA UDI
    FEMSELECT LTD·07290017082028·

    Taurus Pedicle Screw System

    FDA UDI
    SINTX Technologies, Inc.·M555500000102·Taurus Case 1 - Base

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555244000102·Persuader

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555241000102·5.5mm, Poly Screw Driver

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555211000102·Poly Screw Driver - HF

    MAGNA 5000 PHASED ARRAY CTL SPINE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    IMMULITE PHENOBARBITAL, MODELS LKPB1, LKPB5

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    6000102-1999-00007

    FDA Adverse Event
    Injury ·December 17, 1999

    BA KIT,WE,P102,1',BE,P37,INL,6',(BE ONLY

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828139298·BA KIT,WE,P102,1',BE,P37,INL,6',(BE ONLY

    BA KIT,WE,P102,1",BE,S37,INL,1'(N ONLY)

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828156004·BA KIT,WE,P102,1",BE,S37,INL,1'(N ONLY)

    BA KIT,WE,P102,1",BE,P37,INL,1'(N ONLY)

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828156721·BA KIT,WE,P102,1",BE,P37,INL,1'(N ONLY)

    CHAIT PERCUTANEOUS CECOSTOMY CATHETER

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code KNT·February 8, 2013

    SECURE II MED/SURG BED

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

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 19, 2008

    FALLOPIAN TUBE OCCLUSION INSERT

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·May 16, 2025