BEUDAMED
    4,710 results · 43ms · Sources: EU EUDAMED, US FDA

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    Aneroid Kits

    FDA UDI
    RASHMAN CORPORATION·00786511082284·BP-FSO & CLINCIAL LITE W/CASE-CB

    Aneroid Kits

    FDA UDI
    RASHMAN CORPORATION·00786511085902·SB- ANEROID BP-FSO W/CASE & SPRAGUE KIT-BX

    Aneroids (82 etc.)

    FDA UDI
    RASHMAN CORPORATION·00786511086206·SB ANEROID/CLAMSHELL - FSO

    Aneroid Kits

    FDA UDI
    RASHMAN CORPORATION·00786511086503·FLORALSTITCH ORCHID - ANEROID/DUALHEAD

    Aneroids (82 etc.)

    FDA UDI
    RASHMAN CORPORATION·00786511079123·PREMIUM ANEROID BP-BUR-BX

    Aneroids (82 etc.)

    FDA UDI
    RASHMAN CORPORATION·00786511077945·PREMIUM ANEROID BP-FSO-CL

    Aneroid Kits

    FDA UDI
    RASHMAN CORPORATION·00786511079536·ANEROID BP-FSO W/CASE & SPRAGUE KIT-BX

    Aneroids (82 etc.)

    FDA UDI
    RASHMAN CORPORATION·00786511078072·NYLON CUFF W/2-TUBE BLADDER-FSO-BULK

    Aneroids (82 etc.)

    FDA UDI
    RASHMAN CORPORATION·00786511078201·ANEROID BP-FS0 W/CASE-BULK

    Aneroids (82 etc.)

    FDA UDI
    RASHMAN CORPORATION·00786511086060·ANEROID BP-FSO-BULK

    AMPLATZER SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·August 30, 2017

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·September 15, 2023

    FSO CERAMIC SHELLS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. BROOKS MANUFACTURING SITE·Product code JDH·July 31, 2010

    AMPLATZER SEPTAL OCCLUDER

    FDA Adverse Event
    Death ·ABBOTT MEDICAL·Product code MLV·May 23, 2022

    AMPLATZER SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code MLV·May 21, 2022

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 18, 2020

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 2, 2020

    ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·ALARIS MEDICAL SYSTEMS·Product code FPA·November 25, 1997

    REF FSO 5 50MM OD

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·July 15, 2015

    REF FSO 9 70MM OD

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code LPH·March 10, 2025