BEUDAMED
    15 results · 18ms · 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.

    GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Damon 3

    FDA UDI
    ORMCO CORPORATION·00889989003437·U1R DAMON 3 .022 +17/+5/0 SUP/TQ

    SINGLE LUMEN CATHETERS, MODIFICATION

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

    RENAX HEMODIALYSIS BLOOD TUBING SET; SUNDER HEMODIALYSIS BLOOD TUBING SET

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

    CHAMBER COMPLETE AUTOFEED 900

    FDA Adverse Event
    Malfunction ·Product code BTT·May 5, 2021

    CHAMBER COMPLETE AUTOFEED 900

    FDA Adverse Event
    Malfunction ·Product code BTT·January 21, 2020

    PDL IMPLANT

    FDA Adverse Event
    Injury ·Product code HSB·January 14, 2013

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 3, 2010

    ETS LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 3, 2014

    VENTED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·July 17, 2023

    VENTED AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 20, 2023

    VENTED AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·January 23, 2024

    CHAMBER COMPLETE AUTOFEED 900

    FDA Adverse Event
    Malfunction ·Product code BTT·June 3, 2021

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 15, 2024

    CHAMBER COMPLETE AUTOFEED 900

    FDA Adverse Event
    Malfunction ·Product code BTT·February 4, 2021