BEUDAMED
    9 results · 27ms · 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.

    MEDSHIELD/AEROCHAMBER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Edge™ Diamond PS014-8C Parallel Shoulder

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172005593·Diamond dental bur, reusable

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295238751·P.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ ...

    Catalys Precision Laser System

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DORNIER MEDILAS H 20 LASER

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

    ENDOPATH ENDOSCOPIC VASCULAR LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 9, 1996

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·May 29, 2014

    UNKNOWN DEPUY HEAD BALL

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code KWY·February 14, 2013

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 10, 2011