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

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    ARROW REDIGUARD, 9FR. 50CC, INTRA-AORTIC BALLOON VATHETER, IAB-R950-U

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890103301·Zirlux Guide Pin

    integral

    FDA UDI
    Merz Dental GmbH·D7091010330·Living mould chart integral A3 containing: 10 u...

    Everest & Jennings

    FDA UDI
    GF HEALTH PRODUCTS, INC.·M3683K0103301·W/C ADVANT RCL 20X17 DSK ELR

    Intess L

    FDA UDI
    Kalitec Direct LLC·B07312K0100300·Caddie Lid, Lumbar Implants,Hinged

    Matira

    FDA UDI
    Kalitec Direct LLC·B07307K0100300·Caddie Lid, Plates and Screws

    Inseption

    FDA UDI
    Kalitec Direct LLC·B07314KJ0100300·Caddie Lid, ISP Implants, Hinged

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B073DRK0100300·Sagittal Bender, Straight

    SOVEREIGN BIPOLAR INSTRUMENTS

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

    NITRILE PATIENT EXAMINATION GLOVE (GREEN COLOR), POWDER FREE, NON STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TRUSTEEL

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 18, 2025

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    BD ULTRA-FINE 6MM¿ INSULIN SYRINGE 0,5ML 31G X 6MM U-100 10X3COUNT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMI·September 15, 2022

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    ZELTIQ COOLMAX (8.0)

    FDA Adverse Event
    Injury ·ZELTIQ AESTHETICS INC.·Product code OOK·March 14, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·February 11, 2011