BEUDAMED
    18 results · 27ms · 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 ×

    Masimo Rad-67 Pulse CO-Oximeter and Accessories

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PM-1000F+PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCORDION STONE MANAGEMENT DEVICE MODEL AC281205 AND AC3814510

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

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·June 4, 2019

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·October 17, 2014

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 21, 2013

    PRESOURCE CUSTOM STERILE CABG PACK

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code FZP·July 20, 2011

    SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·March 1, 2024

    SHIDEN

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 10, 2020

    Metrotom 800 (130kV CT scanner) Industrial CT scanner for measuring and inspecting complete components made of plastic or light metal.

    FDA Enforcement
    Class II ·Ongoing·Carl Zeiss Metrology Inc·February 7, 2018

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 18, 2022

    SHIDEN

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 2, 2021

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    SHIDEN

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·January 6, 2022

    MUST MINI OC PRE-BENT TRANSITION ROD 75° Ø3.5/4X 200MM (STE)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKG·April 25, 2024