BEUDAMED
    3,180 results · 36ms · 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 ×

    DOUBLE LUMEN SOFT CENTRAL VENOUS CATHETER TRAY

    FDA Adverse Event
    Injury ·COOK INCORPORATED·Product code KRK·January 10, 2002

    CENTRAL VENOUS PRESSURE MONITOR

    FDA Adverse Event
    EDWARDS DIV., BAXTER HEALTHCARE COORP.·Product code KRK·February 28, 1995

    MANOMETER BOTTOM ASSEMBLY

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KRK·May 13, 2022

    MANOMETER, BLOOD-PRESSURE, VENOUS

    FDA Adverse Event
    Malfunction ·VORTECH·Product code KRK·August 12, 2023

    PORTEX MANOMETER

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code KRK·June 22, 2020

    MANOMETER TRAY STERILE 10/BX - 4330

    FDA Adverse Event
    Injury ·Product code KRK·September 27, 2021

    MANOMETER TRAY STERILE 10/BX - 4330

    FDA Adverse Event
    Injury ·CAREFUSION, INC·Product code KRK·August 23, 2021

    MEDEX PRESSURE INFUSION CLEAR CUFF

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code KRK·September 9, 2022

    CUSTOM MONITORING SET

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code KRK·March 30, 2000

    CVP MANOMETER

    FDA Adverse Event
    Injury ·MEDEX·Product code KRK·April 16, 2003

    VENOUS LINE - COBE BAXTER

    FDA Adverse Event
    Injury ·NATIONAL MEDICAL CARE·Product code KRK·August 2, 1993

    STOPCOCK 9 IN EXTENSION

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL CORP.·Product code KRK·March 22, 1996

    SMITHS MEDICAL PORTEX HYPERINFLATION RESUSCITATION MANOMETERS

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code KRK·August 19, 2019

    MANOMETER TRAY STERILE 10/BX

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KRK·September 16, 2019

    DATASCOPE

    FDA Adverse Event
    Injury ·DATASCOPE CORPORATION·Product code KRK·February 11, 1993

    Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H IN4130/JPH IN4130/K IN4130/KRK IN4130/L IN4130/T IN4230/JPH IN4230/K IN4330/CNK IN4330/K IN4352/K IN4430/K IN4530/CNK IN4530/K IN4530/T IN4802/K IN4802/T IN4852/K IN4901/A IN4902/A IN4903/A IN4904/A IN4905/A IN4906/A IN4907/A IN4908 IN4909 IN4910 IN4911/A IN4912 IN4913/A IN4914/A IN4915 IN4916/A IN4917/A IN4918/A IN4919/A

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code PTM·December 4, 2025

    Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H IN4130/JPH IN4130/K IN4130/KRK IN4130/L IN4130/T IN4230/JPH IN4230/K IN4330/CNK IN4330/K IN4352/K IN4430/K IN4530/CNK IN4530/K IN4530/T IN4802/K IN4802/T IN4852/K IN4901/A IN4902/A IN4903/A IN4904/A IN4905/A IN4906/A IN4907/A IN4908 IN4909 IN4910 IN4911/A IN4912 IN4913/A IN4914/A IN4915 IN4916/A IN4917/A IN4918/A IN4919/A

    FDA Enforcement
    Class II ·Ongoing·Merit Medical Systems, Inc.·January 28, 2026

    MX441B, CVP Manometer. The product is packaged in a cardboard box. The units are packed ten (10) per case. The product is labeled on the outer case with a stick-on label that reads in part, ''**medex Dublin, OH 43016 USA**STERILE***MX441B CVP Manometer**Lot#***Latex Free''

    FDA Recall
    Terminated ·Medex Inc·Product code KRK·November 18, 2005

    Manometer, 550 ml three-Way Stopcock; STERILE;

    FDA Recall
    Terminated ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KRK·February 23, 2017

    Manometer, Blood-Pressure, Venous

    FDA classification
    FDA Class 2 ·Manometer, Blood-Pressure, Venous