BEUDAMED
    106 results · 38ms · Sources: EU EUDAMED, US FDA

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    AUTO-BAND LIGATOR

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526780842·LEVAMED ACTIVE ANKLE SUP SLVR R VI

    MODIFICATION TO IMPLANTABLE CLIP

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

    RIZA BAND STRETCHER (RBS)-60000

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

    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

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 4, 2013

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·March 17, 2011

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·April 17, 2008

    CA090, DIRECT DRIVE LCA 3/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code FZP·October 11, 2016

    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

    MONOMEND MAX 3/0 (2) 70CM DS24(M)VPL RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·July 31, 2023