BEUDAMED
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    FDA UDI
    GE Healthcare Japan Corporation·00840682117302·CAE

    Allied Medical LLC

    FDA UDI
    Allied Medical, LLC·00026072000021·Transport Ventilator with Internal Compressor

    OHMEDA-OHIO CAE PLUS INCUBATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Complement Activation (CAE) Reagent Set

    FDA UDI
    Diasorin Inc.·08056771600798·

    Frova Intubating Introducer (C-CAE-14.0-70-FII); Frova Intubating Introducer (C-CAE-14.0-70-FI); Frova Intubating Introducer (C-CAE-14.0-70-FIC); Frova Intubating Introducer (C-CAE-14.0-70-FIC-SPOPS)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    COMPLEMENT ACTIVATION EIA TEST SYSTEM (CAE)

    FDA 510(k)
    FDA Class 2 ·Immunology

    COOK AIRWAY EXCHANGE CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LRC·September 9, 2024

    Complement Activation (CAE) Calibrator and Controls Set

    FDA UDI
    Diasorin Inc.·08056771600804·

    12FR X 68CM ENDOVIVE TTP JEJUNAL FEEDING PIGTAIL TIP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNT·February 24, 2023

    COOK AIRWAY EXCHANGE CATHETERS EF

    FDA Adverse Event
    Injury ·COOK, INC.·Product code BTR·April 27, 2006

    COOK AIRWAY EXCHANGE CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LRC·September 16, 2024

    7IN CAE 16.5 MMA

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·September 23, 2013

    COOK AIRWAY EXCHANGE CATHETER

    FDA Adverse Event
    Death ·COOK, INC.·Product code KTI·March 8, 2013

    Welch Allyn, Inc.

    FDA UDI
    WELCH ALLYN, INC.·00817655020853·H3+ 3-channel digital Holter Recorder - 7-day, ...

    CLOSUREFAST CATHETER

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·November 3, 2025

    AMPLATZER VASCULAR PLUG

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code KRD·September 18, 2025

    AMPLATZER VASCULAR PLUG

    FDA Adverse Event
    Death ·ABBOTT MEDICAL·Product code KRD·September 18, 2025

    RADIOFREQUENCY GENERATOR

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·March 21, 2019

    CLOSUREFAST CATHETER

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·March 21, 2019

    COOK AIRWAY EXCHANGE CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LRC·June 16, 2017