BEUDAMED
    103 results · 22ms · Sources: EU EUDAMED, US FDA

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    SMITH & NEPHEW ULTRABRAID SUTURE

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

    RABEA 0°

    FDA UDI
    SIGNUS Medizintechnik GmbH·04047844000229·The basic shape of the NUBIC and RABEA devices ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694008228·1.2mm x 16mm Lag Screw

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K0142160·Trial, TLIF, 32L OB CRV 7Deg, 16mm

    InSePtion MIS Fixation System

    FDA UDI
    Kalitec Direct LLC·B07314K0112160·Rasp, 16 and 18 mm

    POWDER-FREE LATEX EXAMINATION GLOVE STERILE WITH OPTIONAL PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PVC FREE INTRAVASCULAR ADMINISTRATION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·April 8, 2013

    CD HORIZON LEGACY SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 8, 2008

    PRECISE RX NITINOL STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·April 6, 2011

    CLINITEK STATUS+

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code JHI·December 2, 2019

    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

    MONOPLUS C VIOLET 2/0 (3) 25M

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·January 30, 2019