BEUDAMED
    10 results · 21ms · 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.
    Filters Regulation: Us FDA ×

    CT/MR Compatible M.A.C. Interstitial GYN Template

    FDA 510(k)
    FDA Class 2 ·Radiology

    HHM

    FDA UDI
    Oticon A/S·05707131282521·H110V2, BTE 13 WL 85 CNB HHM

    NITRILE EXAM GLOVE, POWDER-FREE MODEL COLOR WHITE, NITRILE EXAM GLOVE, POWDER-FREE MODEL COLOR BLUE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    S4 SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    S4C POLYAXIAL SCREW 3.5X12MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code MNI·May 1, 2009

    QUADRA-H CEMENTLESS, HA COATED STEM SIZE 0 STD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·March 24, 2017

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 6, 2013

    HIP HEAD, 10/12 TAPER, 28MM,+0MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 29, 2011

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code LFL·August 28, 2008

    VERTEBRAL BODY SET/SMALL- STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code KWQ·August 9, 2021