BEUDAMED
    24 results · 31ms · Sources: EU EUDAMED, US FDA

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    BI-FUNNEL GASTROSTOMY FEEDING TUBE, TRI-FUNNEL GASTROSTOMY FEEDING TUBE

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

    Port Access Needle

    FDA UDI
    Bard Access Systems, Inc.·00801741047466·PowerLoc Max 20G x 0.75 inch

    Equator

    FDA UDI
    Preat Corporation·00842092179963·Equator Abutment for Nobel Active/Conical RP x 1mm

    Port Access Kit

    FDA UDI
    Bard Access Systems, Inc.·00801741044298·PowerLoc MAX 20G x .75" PAK

    Suprasorb

    FDA UDI
    Huizhou Foryou Medical Devices Co., Ltd.·06940610115678·

    PORT ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code FPA·April 9, 2024

    PORT A CATH NEEDLE

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code FPA·September 30, 2024

    VITEK 2 STRPTOCOCCUS AMPICILLIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    QUILL SYNTHETIC ABSORBABLE BARBED SUTURE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    POWERLOC MAX POWER-INJECTIBLE INFUSION SET 20G X 0.75IN

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code FPA·October 22, 2019

    POWERLOC MAX PORT ACCESS KIT 20G X 0.75IN

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code FPA·March 21, 2023

    POWER LOC MAX REF 0142075

    FDA Adverse Event
    Malfunction ·C. R. BARD·Product code FPA·July 17, 2018

    POWERLOC MAX POWER-INJECTIBLE INFUSION SET 20G X 0.75

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code FPA·May 3, 2024

    PORT ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code FPA·September 17, 2024

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 4, 2014

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 3, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·June 28, 2011

    MINILOC SAFETY INFUSION SET 20G X 1 IN

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code FPA·November 14, 2019

    POWERLOC MAX POWER-INJECTIBLE INFUSION SET 20G X 0.75IN

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code FPA·November 14, 2019

    PowerLoc MAX Power Injectable Infusion Port Access Kit; Catalog Numbers 2131910 (UDI 00801741044151), 2131915 (UDI 00801741044168), 2131975 (UDI 00801741044175), 2132010 (UDI 00801741044151), 2132015 (UDI 00801741044199), 2132075 (UDI 00801741044205), 2132210 (UDI 00801741044212), 2132275 (UDI 00801741044236), 2141910 (UDI 00801741044243), 2141915 (UDI 00801741044250), 2141975 (UDI 00801741044267), 2142010 (UDI 00801741044274), 2142015 (UDI 00801741044281), 2142075 (UDI 00801741044298), 2142210 (UDI 00801741044304), 2142215 (UDI 00801741044311), 2142275 (UDI 00801741044328)

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Company·July 29, 2020