BEUDAMED
    120 results · 26ms · Sources: EU EUDAMED, US FDA

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    SURSHIELD SAFETY WINGED INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VITROS IMMUNODIAGNOSTIC PRODUCTS FOLATE REAGENT PACK 1/2, VITAMIN B12/FOLATE REAGENT PACK 3, PRODUCTS RED CELL FOLATE PA

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    RUSCH POLYFLEX STENT KIT

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

    SAFIL VIOLET 8/0 (0.4) 30CM 2XDLM6

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·August 9, 2019

    APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 11, 2015

    APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 11, 2015

    APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 11, 2015

    APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 11, 2015

    INTELLIVUE MULTI MEASURMENT SERVER X2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH, CARDIAC AN·Product code MHX·March 5, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 16, 2011

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·April 18, 2008

    Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x37,5 mm Catalog Number: 18965037S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

    FDA Enforcement
    Class II ·Terminated·Stryker GmbH·June 24, 2020

    MONOPLUS VIOLET 0 (3,5) 90CM HR37S(M)RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.U.·Product code NEW·December 14, 2021

    MONOPLUS C VIOLET 2/0 (3) 25M

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·January 2, 2019

    MONOPLUS VIOLET 4/0 (1.5) 70CM HR17 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·October 23, 2019

    MONOPLUS C VIOLET 2/0 (3) 25M

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·June 2, 2022

    MONOPLUS VIOLET 3/0 (2) 70CM HR22 (M)RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·July 30, 2021

    MONOMEND MAX 2/0 (3)70CM HS37S(M)VPL DDP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·August 13, 2021

    MONOPLUS VIOLET 4/0(1,5)4X45 HR22 TO(M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·October 2, 2019

    SAFIL VIOLET 1 (4) 90CM HR48 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code GAM·November 20, 2019