BEUDAMED
    25 results · 21ms · Sources: EU EUDAMED, US FDA

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    SOFTLINE SPRING CLIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741028755·Catheter Placement Kit

    GEN4 INTERACTIVE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828115339·GEN4 INTERACTIVE

    Ormesh

    FDA UDI
    ORMCO CORPORATION·00889989017335·ORMESH PIX TUBE 18 X 025 X 2MM LONG

    LIFEPAK 15 monitor/defibrillator

    FDA UDI
    PHYSIO-CONTROL, INC.·00883873808245·15AABAABAABBBAAAAAAAAAAFLP15 MONITOR/DEFIB

    LIFEPAK 15 AC Power Adapter

    FDA UDI
    PHYSIO-CONTROL, INC.·07613327666656·ADAPTER, POWER, AC TO DC,ENHANCED, LP15

    Smoke Tubing

    FDA UDI
    I.C. MEDICAL, INC.·00817688021513·

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555244000098·Universal Rod Rocker, Assembly

    Oxygen Sensor

    FDA UDI
    Honeywell Healthcare Solutions GmbH·04036616000482·Oxygen Sensor OOM110

    RENAFLO II HF 2000 HEMOFILTER

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

    BRANEMARK NOVUM

    FDA 510(k)
    FDA Class 2 ·Dental

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·February 26, 2004

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014601243·URO-TRAPPER DRAIN BAGS, STERILE

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·September 18, 2006

    S3 EX - 3005

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 12, 2013

    POSEY KEEPSAFE DELUXE

    FDA Adverse Event
    Malfunction ·J. T. POSEY COMPANY·Product code KMI·February 3, 2011

    SUMMIT DUOFIX TAP SZ5 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·February 18, 2008

    AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

    FDA Recall
    Open, Classified ·Physio-Control, Inc.·Product code MKJ·November 6, 2023

    RESTORE SENSOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 10, 2014

    FLOW-C ANESTHESIA SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code BSZ·December 19, 2024