BEUDAMED
    65 results · 35ms · Sources: EU EUDAMED, US FDA

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    ROSSMAX NON-INVASIVE BLOOD PRESSURE MONITORS, MODELS S380, K350

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809845624·FOR MEN 20-30 MM HG KNEE HIGH OPEN TOE MEDIUM-L...

    HUMPHREY OCT3

    FDA 510(k)
    FDA Class 2 ·Radiology

    YOUNG-HEALTH SUPER EAR THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 3, 2020

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO INC·Product code GJS·October 26, 2010

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·June 3, 2010

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·July 1, 2011

    INRATIO

    FDA Adverse Event
    Other ·ALERE SAN DIEGO, INC.·Product code GJS·October 26, 2010

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·April 11, 2013

    FLEXTEND II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·April 13, 2011

    INJECTION GOLD PROBE BIPOLAR CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·May 23, 2008

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code LXH·March 31, 2017

    EXTENSION SET WITH T-CONN. SL

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·September 21, 2010

    EAR PACK , Model No SFEA12A

    FDA Enforcement
    Class II ·Ongoing·American Contract Systems Inc·March 26, 2025

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code JPA·May 10, 2010

    LS LF IV SET CONVRT PP W/BCCK VLV 2CLAVE

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·April 14, 2011

    LS MICROBR EXT SET

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·August 16, 2010

    Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026

    EXTENSION SET WITH T-CONN. SL

    FDA Adverse Event
    Malfunction ·HOSPIRA, LTD.·Product code FPA·March 15, 2012