BEUDAMED
    9 results · 22ms · 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 ×

    ASC BALANCE MIDDLEWEIGHT GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NOVEON, MODEL LS1100-01-0968

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

    Registrado Scan

    FDA 510(k)
    FDA Class 2 ·Dental

    PRECISION QID

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code NBW·January 26, 2017

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code NBW·January 26, 2017

    PROLIFT PELVIC FLOOR REPAIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTP·February 21, 2013

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MJO·January 27, 2011

    PROFEMUR(R) R PROXIMAL BODY

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·July 31, 2014

    ENDOPATH ENDOSCOPIC MULTIFEED STAPLER

    FDA Adverse Event
    Malfunction ·EES-JUAREZ·Product code GAG·April 16, 1997