BEUDAMED
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    MODULAR RANGE OF RING PROS. FOR HIP REPLACEMENT

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    Disassembly pin for removal of ring cap

    FDA UDI
    Varian Medical Systems Deutschland GmbH·00816389024137·

    Disassembly pin for removal of ring cap

    FDA UDI
    Varian Medical Systems Deutschland GmbH·00816389025417·

    5. OFR URETHANE UMB CATH

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FOS·March 24, 2014

    NEO V-CATH 2 OFR

    FDA Adverse Event
    Malfunction ·NEO MEDICAL INC.·Product code DQY·July 10, 2014

    NEOMED 5.OFR 40 CM PVC

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL, INC.·Product code KNT·December 7, 2020

    PROXIMATE HCS PROCEDURE OFR PROLAPSE AND HEMORRHOIDS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GAG·October 5, 2004

    14 FR SHEATHED CATHETER

    FDA Adverse Event
    CAREFUSION·Product code OFR·December 9, 2010

    KIT,CATHETER,SUCTION,14 FR,WHISTL,2 GLV

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES INC.·Product code OFR·September 23, 2020

    CLEARPRO,CLOSED SXN,14FR,D SWVL,ETT

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, LP·Product code OFR·September 12, 2025

    MEDLINE

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, LP·Product code OFR·May 22, 2026

    AIRLIFE, TRI-FLO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code OFR·June 25, 2008

    CLEARPRO¿ TRACH T-PIECE CLOSED SUCTION CATHETER, 14 FRENCH

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, LP·Product code OFR·May 1, 2026

    PORTEX SUCTIONPRO 72 CLOSED SUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD, INC.·Product code OFR·July 13, 2012

    TRAY,CATHETER,SUCTION,8 FR,2 GLV,MINI

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES LP·Product code OFR·March 7, 2024

    SUCT CTH KIT W/O SOL SFTY-VAC 14FR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code OFR·March 11, 2016

    SUCT CTH KIT W/O SOL SFTY-VAC 10FR

    FDA Adverse Event
    Malfunction ·KENMEX·Product code OFR·March 11, 2016

    BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE KIT

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code OFR·February 27, 2019

    BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE KIT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code OFR·February 7, 2019

    BLUE LINE ULTRA SUCTIONAID TRACHEOSTOMY TUBE KIT

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code OFR·February 27, 2019