BEUDAMED
    2,599 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 ×

    Unimed

    FDA UDI
    Unimed Medical Supplies, Inc.·06936735464364·ECG Monitor Trunk Cable Bionet

    Unimed

    FDA UDI
    Unimed Medical Supplies, Inc.·06936735464593·ECG Monitor Trunk Cable Bionet

    PBN DILATORS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PBN GUIDEWIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PBN DRAINAGE CATHETER GUIDEWIRES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PBN HYSTERO-SALPINGOGRAPHY CATHETER SET

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PBN FALLOPIAN TUBE CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SKATER INTRODUCER SET

    FDA Adverse Event
    Malfunction ·PBN MEDICALS DENMARK A/S·Product code FGE·January 27, 2010

    F7 SKATER NEPHROSTOMY 35 CM

    FDA Adverse Event
    Injury ·PBN MEDICALS DENMARK A/S·Product code FOZ·January 9, 2012

    CANALIZER STANDARD ANGLED

    FDA Adverse Event
    Injury ·PBN MEDICALS DENMARK A/S·Product code DQX·December 9, 2010

    CANALIZER STANDARD STRAIGHT

    FDA Adverse Event
    Injury ·PBN MEDICALS DENMARK A/S·Product code DQX·December 9, 2010

    CANALIZER STIFF ANGLED

    FDA Adverse Event
    Malfunction ·PBN MEDICALS DENMARK A/S·Product code DQX·October 15, 2010

    F6 SKATER SINGLE STEP STRING

    FDA Adverse Event
    Injury ·PBN MEDICALS DENMARK A/S·Product code DQX·December 9, 2010

    SKATER BILIARY

    FDA Adverse Event
    Malfunction ·PBN MEDICALS DENMARK A/S·Product code DQX·May 18, 2011

    MUST PEDICLE SCREWDRIVER - MIS HYBRID

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·December 15, 2017

    POLYAXIAL REDUCTION PEDICLE SCREWDRIVER 2.0 CANNULATED

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·November 20, 2018

    BIOPSY NEEDLE KIT, PASSIVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·June 25, 2015

    BIOPSY NEEDLE KIT, PASSIVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·July 1, 2015

    BIOPSY NEEDLE KIT, PASSIVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·July 1, 2015

    BIOPSY NEEDLE KIT, PASSIVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·July 3, 2015