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

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    PremiPatch PTFE Pledget

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ORTHOPEDIC SALVAGE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304687998·

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00887868267192·

    TERUMO SURGUARD 2 SAFETY NEEDLE OR SIMILAR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    WIRED/ WIRELESS FDR D-EVO WITH X-RAY DETECTION FEATURE

    FDA 510(k)
    FDA Class 2 ·Radiology

    NY-STA BLACK 2/0 18" (45CM) DS24 VPL

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·May 5, 2026

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL ¿ NEUROMODULATION·Product code GZB·October 6, 2014

    CELL-DYN RUBY ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·July 6, 2011

    DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code OJX·June 7, 2013

    SUPRAMID BLACK 3/0 (2) 45CM DS19

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·June 13, 2022

    DAFILON 3/0 (2) 100M

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·December 27, 2023

    SKIN SUTURE PACK DAFILON

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·July 18, 2024

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    SUPRAMID BLACK 4/0 (1.5) 45CM DS16

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·July 17, 2025

    DAFILON 3/0 (2) 100M

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·July 22, 2025

    BD BACTEC¿ PEDS PLUS¿/ F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·March 10, 2023

    SUPRAMID BLACK 4/0 (1.5) 45CM DS19

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·March 10, 2026

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code DQY·December 25, 2016

    SUPRAMID BLACK 3/0 (2) 75CM DS19

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAR·January 11, 2023