BEUDAMED
    18 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 ×

    MICROTAINER BRAND CHEMISTRY TUBES WITH MICROGARD CLOSURE, MODEL 365965, 365985, 365963, 365967, 36578

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MICROTAINER SST GOLD

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·June 7, 2018

    BD MICROTAINER® EDTA LAVENDAR TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·May 1, 2018

    BD MICROTAINER® EDTA LAVENDAR TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·May 16, 2018

    MICROTAINER SST GOLD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD·Product code JKA·May 7, 2018

    BD MICROTAINER® EDTA LAVENDER TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·April 27, 2018

    BD MICROTAINER® EDTA LAVENDAR TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·May 3, 2018

    BD MICROTAINER® BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·December 3, 2017

    CDB FLIP-SIDE-CLIP BRACKET

    FDA 510(k)
    FDA Class 2 ·Dental

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CADD CASSETTE RESERVOIRS - NON FLOW STOP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 13, 2022

    ACCESSORIES

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code DQX·March 20, 2025

    CONSERVE(R) PLUS HA CUP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·March 6, 2013

    VERSA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011

    CUSTOM PACING LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·August 8, 2014

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024

    Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026