BEUDAMED
    8 results · 26ms · 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.

    UNICATH LLU ANGIOGRAPHIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    REPLACEMENT RECHARGEABLE BATTERY PACK'S

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ELECTROSONOGRAM ESG-1

    FDA 510(k)
    FDA Class 1 ·Dental

    TITAN TOUCH

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FHW·July 6, 2022

    VALLEYLAB

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCOHEALTHCARE·Product code GEI·January 28, 2013

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·December 30, 2010

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 21, 2014

    PKG, CLAW FORCEPS, P/N 0250080244. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.

    FDA Enforcement
    Class II ·Terminated·Stryker Endoscopy·December 24, 2014