BEUDAMED
    2,465 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    PERCUTANEOUS CV CATHETER INSERTION KIT W OR W/O CV

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·October 13, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·October 13, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·October 13, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·October 13, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·October 13, 2011

    MICROFIX QA+#3/0 OC V-4

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·May 8, 2024

    MICROFIX QA+#3/0 OC V-4

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·October 28, 2024

    MICROFIX QA+#3/0 OC V-4

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·October 28, 2024

    MICROFIX QA+#3/0 OC V-4

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·October 30, 2024

    MICROFIX QA+#3/0 OC V-4

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·December 23, 2024

    MICROFIX QA+#3/0 OC V-4

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·April 9, 2025

    AUTOMATED IMPELLA CONTROLLER

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·November 8, 2024

    MICROFIX QA+#3/0 OC V-4

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·February 13, 2026

    MICROFIX QA+#3/0 OC V-4

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·February 13, 2026

    MICROFIX QA+#3/0 OC V-4

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·February 13, 2026

    V. MUELLER

    FDA Adverse Event
    Injury ·CAREFUSION·Product code OCV·August 31, 2015

    MH-498 (E) CONNECTING ARM OF SH-1

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code OCV·July 12, 2024

    CONNECTING ARM

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code OCV·April 11, 2026

    CLAMPING JAW, SMALL

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code OCV·April 14, 2023