BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    CONTOR TABLE SURFACE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODEL TW SB, SCALP VEIN SET; MODEL TW LB, STERILE HYPODERMIC NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CARERITE FACE MASK

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

    SX OXYGENATOR W/ HR X COATING

    FDA Adverse Event
    Injury ·TERUMO CARDIOVASCULAR SYSTEMS·Product code DTZ·August 5, 2015

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 17, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 1, 2014

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·July 10, 1997