BEUDAMED
    47 results · 23ms · Sources: EU EUDAMED, US FDA

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    HS/HG PROSTHETIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ARGENCO W

    FDA UDI
    ARGEN CORPORATION, THE·D818100245·Alloy other noble metal

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707092902·BKT 45 F1000 SELF-LIGATING 22 T-22 BH

    Metzenbaum Scissors

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896107434·Metzenbaum Scissors Curved

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694033220·15MM RIGHT L RIGID PLATE & 15MM LEFT L RIGID PL...

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780466659·Integra® Jarit® Lillehei-Potts Scissors, 7", Cu...

    NorthStar

    FDA UDI
    Seaspine Orthopedics Corporation·10889981199395·4.5mm Tap

    CSM STRETTA SYSTEM

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

    ACTIVHEAL SCAR MANAGEMENT DRESSING

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Tether™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981035525·Plate - 2 Level - 45mm

    SET, ADMINISTRATION, INTRAVASCULAR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2016

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, MEDIUM, 12°

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 4, 2024

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 8, 2013

    VALIANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·September 18, 2014

    9900

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

    STOPCOCK MANIFOLD GANGS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FMG·June 17, 2020

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, LARGE, 12°, STERILE, SINGLE USE

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAS·May 24, 2023

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, LARGE, 30°, STERILE, SINGLE USE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·June 6, 2023

    HF-RESECTION ELECTRODE, LOOP

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAS·June 2, 2023

    SMR REVERSE HUMERAL BODY SHORT

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·April 5, 2022