BEUDAMED
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    KNEEKG

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TS 7500

    FDA UDI
    Baxter Medical Systems GmbH + Co. KG·00887761968639·TruSystem 7500

    TRUMPF MEDICAL

    FDA UDI
    Baxter Medical Systems GmbH + Co. KG·00887761984455·TruSystem 7500

    RCT Resorbable Collagen Tape

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950008148·*SPECIAL ORDER* RCT COLLAGEN TAPE 7.5X2.5CMX1MM...

    RCT Resorbable Collagen Tape

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950007233·RCT COLLAGEN TAPE 1MM THICK 2.5CM X 7.5CM RESOR...

    RCT

    FDA UDI
    COLLAGEN MATRIX, INC.·00813954027883·Resorbable Collagen Tape

    NIOX MINO MODEL 09-1000

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702356991·Elvarex 2/Knee High/Slant-Open Toe/Dotted silic...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702429923·Elvarex 1/Thigh High/Slant-Closed Toe/Thigh hig...

    CMORE® System, Nut Screw, Ti

    FDA UDI
    icotec AG·07640172553541·CMORE® System, Nut Screw, Ti

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702247275·Elvarex 2/Thigh High/Profile, Closed Toe, Knee ...

    Immunalysis

    FDA UDI
    IMMUNALYSIS CORP·00840937105207·Amphetamine Antibody Analyte Specific Reagent (...

    TRAM 2001 MODULE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SHANGHAI GLOVMAX ENTERPRISE POWDERED BLUE NITRILE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·September 8, 2015

    TEGO CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·June 19, 2025

    LEAD EXTRACTION EVOLUTION SHORTIE RL CONTROLLED-ROTATION DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DRE·September 9, 2015

    I-STAT ACT KAOLIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JBP·March 14, 2013

    Baxter TruSystem 7500, Product Code 4091000

    FDA Recall
    Open, Classified ·Baxter Healthcare Corporation·Product code GDC·February 25, 2025

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 2, 2013