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

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    CAREVENT

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

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496062240·SCOTTISH KNEE-HIGH 100 UNISEX, SIZE L, BLU NAVY...

    RN Screw-retained Abutment Analog,Φ4.8mm

    FDA UDI
    BIO CONCEPT Co., Ltd.·06947600304593·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X0622400·6mm H x 22mm W x 40mm L x 0 degrees XLIF

    SANUWAVE, INC.

    FDA registration
    SANUWAVE, INC.·3 products·🇺🇸 United States

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X06224080·6mm H x 22mm W x 40mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X062240120·6mm H x 22mm W x 40mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L062240120·6mm H x 22mm W x 40mm L XLIF Trial 12 degree Lo...

    RENDER-PLAN 3-D 4.00 & PRECISE-PLAN 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    MERTEX-PLUS O.R./SURGEONS GOWN, NONSTERILE

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

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code DTK·August 21, 2014

    UNK

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DTK·August 20, 2014

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·August 20, 2014

    WALLSTENT (ILIAC, TIPS, VENOUS) ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code MAF·April 16, 2013

    RSP SHOULDER INSTRUMENT

    FDA Adverse Event
    Malfunction ·ENCORE MEDICAL, L.P.·Product code HWX·March 17, 2011

    LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·June 17, 2008

    GUNTHER TULIP VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·April 3, 2026

    JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G X 1/2" (0.33mm x 13mm), REF 4428-1 b) 1.0mL 29G X 1/2" (0.33mm x 13mm), REF 4429-1

    FDA Enforcement
    Class I ·Terminated·Smiths Medical ASD Inc.·June 16, 2021

    DXTEND GLENOSPHERE STD D42MM

    FDA Adverse Event
    Injury ·DEPUY FRANCE·Product code KWS·December 6, 2012

    GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·September 12, 2017