BEUDAMED
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    FIB Calibrator

    FDA UDI
    R 2 DIAGNOSTICS, INC.·10859394006191·Fibrinogen Reference Plasma 10 x 1 ml

    Tools - AFS

    FDA UDI
    Trimed, INC.·00842188110382·AFS Fibula Caddy

    FIBROTEK FIB

    FDA 510(k)
    FDA Class 2 ·Hematology

    SAF-D-FIB

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PORTA-FIB LPD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PORTA FIB III

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Tools - AFS

    FDA UDI
    Trimed, INC.·00842188126888·AFS Fibula Caddy Lid

    ROTEM®

    FDA UDI
    Tem Innovations GmbH·04260160470075·The FIBTEM assay is a semi-quantitative in vitr...

    ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL

    FDA 510(k)
    FDA Class 1 ·Radiology

    SPQ TEST SYSTEM II FOR FIB (SERUM PROTEIN QUANTI.)

    FDA 510(k)
    FDA Class 2 ·Hematology

    MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Sonoma Orthopedic Products, Inc.

    FDA UDI
    ARTHREX, INC.·00816988012368·

    EX-TEM. FIB-TEM, AND AP-TEM FOR ROTEM DELTA THROMBOELASTOMETRY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    ARRHYTHMIA MONITORING SOFTWARE

    FDA Adverse Event
    Injury ·HEWLETT-PACKARD CO.·Product code DRT·April 14, 1995

    SAF-D-FIB

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code DRK·October 5, 1994

    PHYSIO-CONTROL

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL·Product code LDD·August 11, 1999

    PU-681RA

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·October 10, 2023

    CNS-6201A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·September 5, 2020

    BCS XP SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GKP·January 10, 2019

    BCS XP SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GKP·January 10, 2019