BEUDAMED
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    CKG CARDIOKYMOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CKG 8800

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CKG 8000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SERIES 602 CKG RECORDER (MODIFIED)

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    MULTI-LINK RX PENTA CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·GUIDANT VASCULAR INTERVENTION CARDIOVASCULAR SYSTE·Product code MAF·September 9, 2004

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·September 20, 2016

    IMMULITE 2000 ACTH

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CKG·October 19, 2016

    ST AIA-PACK 27.29

    FDA Adverse Event
    Injury ·TOSOH AIA, INC.·Product code CKG·April 9, 2012

    ELECSYS ACTH

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CKG·December 29, 2025

    IMMULITE 2000 XPI

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code CKG·August 8, 2011

    ELECSYS ACTH

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CKG·September 21, 2023

    ELECSYS ACTH

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CKG·August 7, 2025

    ELECSYS ACTH TEST SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CKG·April 13, 2020

    ELECSYS ACTH

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CKG·June 5, 2024

    ACTH, CHEMILUMINISCENCE KIT

    FDA Adverse Event
    Malfunction ·NICHOLS INSTITUTE DIAGNOSTICS·Product code CKG·October 24, 2006

    IMMULITE 2000 ACTH

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code CKG·January 30, 2017

    ELECSYS ACTH

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CKG·July 25, 2022

    ELECSYS ACTH

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CKG·January 31, 2023

    ELECSYS ACTH TEST SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CKG·November 21, 2016

    IMMULITE 2000

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code CKG·September 15, 2009