BEUDAMED
    7 results · 18ms · 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.

    BLADDER KIT - 734000

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

    TEMP. PROBE, & ELECTRONIC THERMOMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NuVasive® Modulus TLIF Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROG VALVE INLINE W SG

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·August 6, 2021

    FLEXCATH ADVANCE STEERABLE SHEATH

    FDA Adverse Event
    Malfunction ·MEDTRONIC CRYOCATH LP·Product code DRA·April 25, 2014

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·October 2, 2012

    TROCH ENTRY LH 12MMX34CM

    FDA Adverse Event
    Injury ·DEPUY ACE S.A. 'R.L.·Product code HSB·July 23, 2010