BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    ECOGEL 200 ULTRASOUND GEL

    FDA 510(k)
    FDA Class 2 ·Radiology

    3M™ Victory Series™

    FDA UDI
    3M UNITEK CORPORATION·00652221118288·3M™ Victory Series™ Second Molar Bands, 955-246...

    Zuma™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981060626·Trial, 26mm x 24mm x 16mm, 12 Deg

    AURORA M MEDICAL DYE LASER

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

    CONVEEN(R) URISHEATH AND URILINER(MALE EXTER CATH)

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    LARYNG-O-JET KIT

    FDA Adverse Event
    Injury ·Product code FMF·June 20, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 11, 2013

    RIATA ST OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    Zeiss brand IOLMaster, Version 1-5, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufactured by Carl Zeiss Meditec AG (Jena), Carl Zeiss Promenade 10, Jena, Germany 07745; and distributed by Carl Zeiss Meditec, Inc., Dublin, CA This device is intended for use primarily by physicians and health care workers and may be only used under the supervision of a physician. This device will not be sold to the general public. The IOLMaster is intended for the biometric determination of ocular measurements of axial length, anterior chamber depth, corneal radius, white-to white (WTW), and for the measurement of pupil size and deviation of the visual axis from the center of the pupil. For patients who are candidates for intraocular lens (IOL) implantation, the device also performs calculations to assist physicians in determining the appropriate IOL power and type for implantation

    FDA Enforcement
    Class II ·Terminated·Carl Zeiss Meditec, Inc.·November 27, 2013