BEUDAMED
    24 results · 32ms · Sources: EU EUDAMED, US FDA

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    MYTHOS 500

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526159532·PROTECT.EPI ELBOW SUPPORT GRAY V

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496030805·FRESH, SIZE XXL, NERO, MICRO-MASSAGING SHORTS W...

    Kleegman Teflon Dilator

    FDA UDI
    MEDGYN PRODUCTS, INC.·M803030805·Kleegman Teflon Dilator 12" (305mm)

    Catamaran Sacroiliac Joint Fixation System (CAT SIJ Fixation System)

    FDA UDI
    TENON MEDICAL, INC.·B74240308050·7.5mm Center Punch

    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    GYNECOLOGICAL LAPAROSCOPES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    KAVO K.E.Y. LASER 1242

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

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

    *

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019

    9616240-2006-00346

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 2, 2013

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·March 4, 2011

    PIN PLACEMENT GUIDE

    FDA Adverse Event
    Malfunction ·EBI·Product code FZX·April 17, 2008

    Easy Go Vac Aspirator, Model PM65HG. Portable suction unit

    FDA Recall
    Terminated ·Precision Medical, Inc.·Product code BTA·November 9, 2004