BEUDAMED
    8 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.

    ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    C-STEM

    FDA UDI
    DEPUY INTERNATIONAL LTD·10603295235514·C-STEM BROACH SIZE 4

    TROJAN NIRVANA COLLECTION LUBRICATED CONDOMS

    FDA Adverse Event
    Injury ·CHURCH & DWIGHT CO., INC.·Product code HIS·June 24, 2020

    PLEX Elite 9000 SS-OCT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PORTEX NEEDLE-PRO EDGE SAFETY WITH SYRINGE, MODELS 432310, 432210, 432510, 432558

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC·Product code FNL·January 17, 2013

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·January 11, 2011

    EPIDURAL NEEDLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 15, 2014