BEUDAMED
    17 results · 29ms · Sources: EU EUDAMED, US FDA

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    MANGAR BOOSTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VuePoint

    FDA UDI
    Nuvasive, Inc.·00887517179784·VuePoint Screw, 4x14mm Multi Axial

    HEAT LOOP

    FDA UDI
    Biomet Orthopedics, LLC·00880304406612·

    COLUMNMATE (AUTOMATED COLUMN SYSTEM) 1580, 1581

    FDA 510(k)
    FDA Class 2 ·Hematology

    OPTI-RAY SUNGLASSES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    11/13 S-ROM 40MM M SPEC + 0

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code LPH·November 19, 2010

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 9, 2013

    INCEPTA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 14, 2020

    Heat Loop cautery instrument, EO sterile - single use only; Arthrotek Ref. No. 905414 and Biomet Ref. No. 450026.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code GEI·July 12, 2004

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 3, 2024

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    SYRINGE FLU PLUS 0.25-1ML VAR DOSE 25X1

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·July 1, 2021

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·January 24, 2023

    RADIFOCUS ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·September 26, 2018