BEUDAMED
    2,279 results · 27ms · Sources: EU EUDAMED, US FDA

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    FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE CHINA

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. Specifically the T210 Treadmill is intended for use in Exercise Testing, facilitating accurate blood pressure measurements and exercise testing within speed range of 0-13.5 miles per hour.

    FDA Recall
    Terminated ·GE Medical Systems Ultrasound & Primary Care Diagnostics, LL·Product code IOL·April 2, 2018

    FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    TRACKMASTER, TREADMILL GE T2100-ST2 220V, MODEL NUMBER 317-07927GE

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    TRACKMASTER, TREADMILL TMX428CP 220V, MODEL NUMBER 317-07929

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·May 12, 2023

    Accessory shorts for the AlterG Anti-Gravity treadmill. Use with the AlterG Anti-Gravity Treadmill for rehabilitation.

    FDA Recall
    Terminated ·AlterG, Incorporated·Product code IOL·January 28, 2014

    GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002 Rev C, or 2028038-008 Rev B. Also Field Replaceable Unit P/Ns 408930-001 Rev E, 408930-002 Rev C. UPDATE: 3-30-2015: T2100 & T2000 Treadmills with power cord part numbers 408930-001, 408930-002, or 2028038-008 Also Field Replaceable Unit P/Ns 408930-001, 408930-002 Product Usage: Used for Exercise Testing, facilitating accurate blood pressure measurements and exercise testing within speed range of 0-13.5 miles per hour.

    FDA Recall
    Terminated ·GE Healthcare·Product code IOL·February 16, 2015

    GE Healthcare, Treadmill T2100. For Exercise Testing, facilitating accurate blood pressure measurements and exercise testing within speed range of 0-13.5 miles per hour.

    FDA Recall
    Terminated ·GE Healthcare·Product code IOL·March 12, 2015

    FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 110V, Model #317-07928

    FDA Recall
    Open, Classified ·Full Vision Inc·Product code IOL·August 31, 2022

    Vial2BAG DC 20mm: 1) REF 6070112 & 2) REF 6070112C, Single use only, Rx Only

    FDA Enforcement
    Class I ·Terminated·WEST PHARMA. SERVICES IL, LTD·February 6, 2019

    Vial2BAG Transfer Device, REF 6070104, Single use only, Rx Only

    FDA Enforcement
    Class I ·Terminated·WEST PHARMA. SERVICES IL, LTD·February 6, 2019

    Vial2BAG DC 13mm, REF 6070111, Single use only, Rx Only

    FDA Enforcement
    Class I ·Terminated·WEST PHARMA. SERVICES IL, LTD·February 6, 2019

    Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness

    FDA classification
    FDA Class 2 ·Device To Detect And Identify Selected Microbial Agents That Cause Acute Febrile Illness

    Assay To Measure Pct To Aid In The Risk Assessment Of Critically Ill Patients On Their First Day Of Icu Admission

    FDA classification
    FDA Class 2 ·Assay To Measure Pct To Aid In The Risk Assessment Of Critically Ill Patients On Their First Day Of Icu Admission